WO2000049181A1 - Procede multiplex de detection d'acides nucleiques - Google Patents

Procede multiplex de detection d'acides nucleiques Download PDF

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Publication number
WO2000049181A1
WO2000049181A1 PCT/US2000/004243 US0004243W WO0049181A1 WO 2000049181 A1 WO2000049181 A1 WO 2000049181A1 US 0004243 W US0004243 W US 0004243W WO 0049181 A1 WO0049181 A1 WO 0049181A1
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WIPO (PCT)
Prior art keywords
nucleic acid
seq
probe
probes
nucleotides
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PCT/US2000/004243
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English (en)
Inventor
Martin K. Lewis
Daniel Kephart
Richard B. Rhodes
John W. Shultz
Donna Leippe
Michelle Mandrekar
Christine Ann Andrews
James R. Hartnett
Trent Gu
Keith V. Wood
Roy Welch
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Promega Corporation
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Publication date
Priority claimed from US09/252,436 external-priority patent/US6159693A/en
Priority claimed from PCT/US1999/005304 external-priority patent/WO1999046409A1/fr
Priority claimed from US09/358,972 external-priority patent/US6235480B1/en
Priority claimed from US09/406,064 external-priority patent/US6270973B1/en
Application filed by Promega Corporation filed Critical Promega Corporation
Priority to AU30019/00A priority Critical patent/AU774085B2/en
Priority to EP00908726A priority patent/EP1155150A1/fr
Priority to CA002357011A priority patent/CA2357011A1/fr
Priority to JP2000599904A priority patent/JP2003535568A/ja
Publication of WO2000049181A1 publication Critical patent/WO2000049181A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6813—Hybridisation assays
    • C12Q1/6827—Hybridisation assays for detection of mutation or polymorphism
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6813—Hybridisation assays
    • C12Q1/6816—Hybridisation assays characterised by the detection means
    • C12Q1/6823—Release of bound markers

Definitions

  • the invention relates to nucleic acid detection. More specifically, the invention relates to the determination of the presence or absence of multiple targeted, predetermined nucleic acid sequences in nucleic acid target/probe hybrids, and the various applications of their detection.
  • nucleic acids or specific nucleic acids are often a portion of a process rather than an end in itself.
  • detection of nucleic acids There are many applications of the detection of nucleic acids in the art, and new applications are always being developed.
  • the ability to detect and quantify nucleic acids is useful in detecting microorganisms, viruses and biological molecules, and thus affects many fields, including human and veterinary medicine, food processing and environmental testing.
  • detection and/or quantification of specific biomolecuies from biological samples e.g. tissue, sputum, urine, blood, semen, saliva
  • forensic science such as the identification and exclusion of criminal suspects and paternity testing as well as medical diagnostics.
  • RNA detection method that is not sequence specific, but is RNA specific is described in U.S. Patent No. 4,735,897, where RNA is depoiyme ⁇ zed using a polynucleotide phosphorylase (PNP) in the presence of phosphate or using a ribonuclease . PNP stops depolymerizing at or near a double-stranded RNA segment. Sometimes double -stranded RNA can occur as a type of secondary structure RNA, as is common in ribosomal RNA, transfer RNA, viral RNA, and the message portion of mRNA.
  • PNP polynucleotide phosphorylase
  • ADP PNP depolymerization of the polyadenylated tail of mRNA in the presence of inorganic phosphate
  • AMP PNP depolymerization using a ribonuclease
  • the formed AMP is converted to ADP with myokinase, and ADP is converted into ATP by pyruvate kinase or creatine phosphokinase .
  • Either the ATP or the byproduct from the organophosphate co- reactant (pyruvate or creatine) is detected as an indirect method of detecting mRNA.
  • ATP is detected by a luciferase detection system.
  • luciferase catalyzes the oxidation of luciferin, producing light that can then be quantified using a luminometer.
  • Additional products of the reaction are AMP, pyrophosphate and oxyluciferin .
  • Duplex DNA can be detected using intercalating dyes such as ethidium bromide. Such dyes are also used to detect hybrid formation.
  • Hybridization methods to detect nucleic acids are dependent upon knowledge of the nucleic acid sequence. Many known nucleic acid detection techniques depend upon specific nucleic acid hybridization in which an oligonucleotide probe is hybridized or annealed to nucleic acid in the sample or on a blot, and the hybridized probes are detected.
  • a traditional type of process for the detection of hybridized nucleic acid uses labeled nucleic acid probes to hybridize to a nucleic acid sample. For example, in a Southern blot technique, a nucleic acid sample is separated in an agarose gel based on size and affixed to a membrane, denatured, and exposed to the labeled nucleic acid probe under hybridizing conditions.
  • probes used in Southern blots have been labeled with radioactivity, fluorescent dyes, digoxygenin, horseradish peroxidase, alkaline phosphatase and acridinium esters .
  • PCR polymerase chain reaction
  • nucleic acid primers complementary to opposite strands of a nucleic acid amplification target sequence, are permitted to anneal to the denatured sample.
  • a DNA polymerase typically heat stable
  • the process is repeated to amplify the nucleic acid target. If the nucleic acid primers do not hybridize to the sample, then there is no corresponding amplified PCR product.
  • the PCR primer acts as a hybridization probe.
  • PCR- based methods are of limited use for the detection of nucleic acid of unknown sequence.
  • the amplified nucleic acid product may be detected in a number of ways, e.g. incorporation of a labeled nucleotide into the amplified strand by using labeled primers.
  • Primers used in PCR have been labeled with radioactivity, fluorescent dyes, digoxygenin, horseradish peroxidase, alkaline phosphatase, acridinium esters, biotin and jack bean urease .
  • PCR products made with unlabeled primers may be detected in other ways, such as electrophoretic gel separation followed by dye- based visualization.
  • U.S. Patent No. 5,582,989 discloses the simultaneous detection of multiple known DNA sequence deletions.
  • the technique disclosed therein uses a first set of probes to hybridize to the targets. Those probes are extended if the targets are present. The extension products are amplified using PCR.
  • Fluorescence techniques are also known for the detection of nucleic acid hybrids
  • U.S. Patent No. 5,691,146 describes the use of fluorescent hybridization probes that are fluorescence-quenched unless they are hybridized to the target nucleic acid sequence.
  • U.S. Patent No. 5,723,591 describes fluorescent hybridization probes that are fluorescence-quenched until hybridized to the target nucleic acid sequence, or until the probe is digested.
  • Such techniques provide information about hybridization, and are of varying degrees of usefulness for the determination of single base variances in sequences.
  • Some fluorescence techniques involve digestion of a nucleic acid hybrid in a 5 ' —»3 ' direction to release a fluorescent signal from proximity to a fluorescence quencher, for example, TaqMan " (Perkin Elmer; U.S. Patent No. 5,691,146 and No. 5, 876, 930) .
  • Enzymes having template-specific polymerase activity for which some 3 ' -»5 ' depolymerization activity has been reported include E. coli DNA Polymerase (Deutscher and Kornberg, J " . Biol . Chem . , 244 (11) :3019-28 (1969)), T7 DNA Polymerase (Wong et al . , Biochemistry 30:526-37 (1991); Tabor and
  • SNPs single nucleotide polymorphisms
  • SNPs are DNA point mutations or insertions/deletions that are present at measurable frequencies in the population. SNPs are the most common variations in the genome. SNPs occur at defined positions within genomes and can be used for gene mapping, defining population structure, and performing functional studies. SNPs are useful as markers because many known genetic diseases are caused by point mutations and insertions/deletions. Some SNPs are useful as markers of other disease genes because they are known to cosegregate .
  • differential sensitivity of the amplified DNA to cleavage can be used for SNP detection.
  • This technique requires that an appropriate restriction enzyme site be present or introduced in the appropriate sequence context for differential recognition by the restriction endonuclease. After amplification, the products are cleaved by the appropriate restriction endonuclease and products are analyzed by gel electrophoresis and subsequent staining. The throughput of analysis by this technique is limited because samples require processing, gel analysis, and significant interpretation of data before SNPs can be accurately determined.
  • Single strand conformational polymorphism is a second technique that can detect SNPs present in an amplified DNA segment (Hayashi, K. Genetic Analysis : Techniques and Applications 9:73- 79, 1992) .
  • the double stranded amplified product is denatured and then both strands are allowed to reanneal during electrophoresis in non-denaturing polyacrylamide gels.
  • the separated strands assume a specific folded conformation based on intramolecular base pairing.
  • the electrophoretic properties of each strand are dependent on the folded conformation.
  • amplification refractory mutation system also known as allele specific PCR or ASPCR
  • two amplification reactions are used to determine if a SNP is present in a DNA sample.
  • Both amplification reactions contain a common primer for the target of interest.
  • the first reaction contains a second primer specific for the wild type product which will give rise to a PCR product if the wild type gene is present in the sample.
  • the second PCR reaction contains a primer that has a single nucleotide change at or near the 3 ' end that represents the base change that is present in the mutated form of the D ⁇ A.
  • the second primer in conjunction with the common primer, will only function in PCR if genomic D ⁇ A that contains the mutated form of genomic D ⁇ A is present.
  • This technique requires duplicate amplification reactions to be performed and analyzed by gel electrophoresis to ascertain if a mutated form of a gene is present. In addition, the data must be manually interpreted.
  • Single base extension is a technique that allows the detection of SNPs by hybridizing a single strand DNA probe to a captured DNA target (Nikiforov, T. et al . Nucl Acids Res 22 :4167-4175) . Once hybridized, the single strand probe is extended by a single base with labeled dideoxynucleotides . The labeled, extended products are then detected using colorimetric or fluorescent methodologies .
  • a variety of technologies related to realtime (or kinetic) PCR have been adapted to perform SNP detection. Many of these systems are platform based, and require specialized equipment, complicated primer design, and expensive supporting materials for SNP detection.
  • the process of this invention has been designed as a modular technology that can use a variety of instruments that are suited to the throughput needs of the end-user.
  • the coupling of luciferase detection sensitivity with standard oligonucleotide chemistry and well-established enzymology provides a flexible and open system architecture.
  • Alternative analytical detection methods such as mass spectroscopy, HPLC, and fluorescence detection methods can also be used in the process of this invention, providing additional assay flexibility.
  • SNP detection using real-time amplification relies on the ability to detect amplified segments of nucleic acid as they are during the amplification reaction.
  • a variety of dyes are known to exhibit increased fluorescence in response to binding double stranded DNA. This property is utilized in conjunction with the amplification refractory mutation system described above to detect the presence of SNP.
  • thermostable polymerases such as Tag to cleave dual- labeled probes present in the amplification reaction
  • the probes used in this assay are distinct from the PCR primer and are dually- labeled with both a molecule capable of fluorescence and a molecule capable of quenching fluorescence.
  • the molecular beacon technology utilizes hairpin-shaped molecules with an internally-quenched fluorophore whose fluorescence is restored by binding to a DNA target of interest (Kramer, R. et al . Nat . Biotechnol . 14:303-308, 1996). Increased binding of the molecular beacon probe to the accumulating PCR product can be used to specifically detect S ⁇ Ps present in genomic D ⁇ A.
  • a final, general fluorescent detection strategy used for detection of S ⁇ P in real time utilizes synthetic D ⁇ A segments known as hybridization probes in conjunction with a process known as fluorescence resonance energy transfer
  • FRET Fluorescence Reactivation
  • a method of this invention is used to determine the presence or absence of a plurality of predetermined (known) nucleic acid target sequences in a nucleic acid sample.
  • Such a method utilizes an enzyme that can depolymerize the 3 ' -terminus of an oligonucleotide probe hybridized to a nucleic acid target sequence to release one or more identifier nucleotides whose presence or absence can then be determined.
  • One embodiment of the invention contemplates a method for determining the presence or absence of a plurality of predetermined nucleic acid target sequences in a nucleic acid sample. Thus, the presence or absence of at least two predetermined nucleic acid target sequence is sought to be determined. This embodiment comprises the following steps .
  • a treated sample may contain a plurality of predetermined nucleic acid target sequences hybridized with their respective nucleic acid probes that include an identifier nucleotide in the 3 ' -terminal region.
  • the treated sample is admixed with a depolymerizing amount of an enzyme whose activity is to release one or more identifier nucleotides from the 3 ' -terminus of a hybridized nucleic acid probe to form a treated reaction mixture .
  • the treated reaction mixture is maintained under depoly erizing conditions for a time period sufficient to permit the enzyme to depolymerize hybridized nucleic acid and release identifier nucleotides therefrom.
  • An analytical output is obtained by analyzing for the presence or absence of released identifier nucleotides, preferably such that the probe from which the nucleotide was released is distinguishable.
  • the analytical output indicates the presence or absence of the nucleotide at the predetermined regions of the nucleic acid targets, and, thereby, the presence or absence of the nucleic acid targets.
  • an analytical output of the methods of the invention can be obtained in a variety of ways .
  • the analytical output can be ascertained by luminescence.
  • analysis for released 3'- terminal region identifier nucleotides comprises the detection of ATP, either by a luciferase detection system (luminescence) or an NADH detection system (absorbance spectroscopy) .
  • ATP molecules are formed from the nucleotide triphosphates released by the depolymerizing step by a phosphate transferring step, for example using an enzyme such as NDPK (Nucleotide Diphosphate Kinase) in the presence of ADP.
  • the ATP is amplified to form a plurality of ATP molecules.
  • typically the enzyme (NDPK) for converting nucleotides and added ADP into ATP is present in the depolymerization reaction, and thus they are denoted as a "one pot" method.
  • the analytical output is obtained by fluorescence spectroscopy.
  • fluorescence detection methods use of a wide variety of fluorescence detection methods is contemplated.
  • an identifier nucleotide includes a fluorescent label .
  • An identifier nucleotide can be fluorescently labeled prior to, or after, release of the identifier nucleotide. It is also contemplated that other than a released identifier nucleotide contains a fluorescent tag.
  • the release of nucleotides in a process of the invention is ascertained by a determination of a difference in the length of the polynucleotide probe, for example by capillary electrophoresis imaged by a fluorescent tag at the 5 ' terminus of the probe or in a region other than the 3' terminal region.
  • the analytical output is obtained by mass spectrometry.
  • an identifier nucleotide be a nucleotide analog or a labeled nucleotide and have a molecular mass that is different from the mass of a usual form of that nucleotide, although a difference in mass is not required.
  • the analytical output can also be obtained by mass spectrometry . It is also contemplated that the analysis of released nucleotides be conducted by ascertaining the difference in mass of the probe after a depolymerization step of a process of the invention.
  • the analytical output is obtained by absorbance spectroscopy.
  • absorbance spectroscopy Such analysis monitors the absorbance of light in the ultraviolet and visible regions of the spectrum to determine the presence of absorbing species.
  • released nucleotides are separated from hybridized nucleic acid and other polynucleotides by chromatography (e.g. HPLC or GC) or electrophoresis (e.g. PAGE or capillary electrophoresis) .
  • chromatography e.g. HPLC or GC
  • electrophoresis e.g. PAGE or capillary electrophoresis
  • Either the released identifier nucleotides or the remainder of the probe can be analyzed for to ascertain the release of the identifier nucleotide in a process of the invention.
  • a label may be incorporated in the analyzed nucleic acid.
  • a sample to be assayed is admixed with two or more nucleic acid probes under hybridizing conditions to form a hybridization composition.
  • the 3' -terminal region of a nucleic acid probe hybridizes with partial or total complementarity to the nucleic acid target sequence when that sequence is present in the sample.
  • the 3 ' -terminal region of the nucleic acid probe includes an identifier nucleotide.
  • the hybridization composition is maintained under hybridizing conditions for a time period sufficient to form a treated sample that may contain said predetermined nucleic acid target sequence hybridized with a nucleic acid probe.
  • the treated sample is admixed with a depolymerizing amount of an enzyme whose activity is to release one or more nucleotides from the 3 ' -terminus of a hybridized nucleic acid probe to form a treated reaction mixture.
  • the treated reaction mixture is maintained under depolymerizing conditions for a time period sufficient to permit the enzyme to depolymerize hybridized nucleic acid and release identifier nucleotides therefrom.
  • the presence of released identifier nucleotides is analyzed to obtain an analytical output, the analytical output indicating the presence or absence of the nucleic acid target sequence.
  • the analytical output may be obtained by various techniques as discussed above.
  • One method of the invention contemplates interrogating the presence or absence of a specific bases in their nucleic acid target sequences in a sample to be assayed, and comprises the following steps.
  • a hybridization composition is formed by admixing a sample to be assayed with a plurality of nucleic acid probes under hybridizing conditions.
  • the sample to be assayed may contain a nucleic acid target sequence to be interrogated.
  • the nucleic acid target comprises at least one base whose presence or absence is to be identified.
  • the hybridization composition includes a plurality of nucleic acid probes that are each substantially complementary to a nucle c acid target sequence of interest and each probe comprises at least one predetermined nucleotide at an interrogation position, and an identifier nucleotide in the 3 ' -terminal region.
  • a treated sample is formed by maintaining the hybridization composition under hybridizing conditions for a time period sufficient for base pairing to occur for all probes when a probe nucleotide at an interrogation position is aligned with a base to be identified in its target sequence.
  • a treated reaction mixture is formed by admixing the treated sample with an enzyme whose activity is to release one or more identifier nucleotides from the 3' -terminus of a hybridized nucleic acid probe to depolymerize the hybrid.
  • the enzymes that can be used in this reaction are further discussed herein.
  • the treated reaction mixture is maintained under depolymerizing conditions for a time period sufficient to permit the enzyme to depolymerize the hybridized nucleic acid and release an identifier nucleotide .
  • An analytical output is obtained by analyzing for the presence or absence of released identifier nucleotides.
  • the analytical output indicates the presence or absence of the specific base or bases to be identified.
  • the analytical output is obtained by various techniques, as discussed herein.
  • an identifier nucleotide is at the interrogation position.
  • one is able to determine if at least one of the plurality of targets is present in the sample.
  • one is able to determine which of the plurality of targets are present and which are absent .
  • a method that identifies the particular base present at an interrogation position optionally comprises a first probe, a second probe, a third probe, and a fourth probe.
  • An interrogation position of the first probe comprises a nucleic acid residue that is a deoxyadenosine or adenosine residue.
  • An interrogation position of the second probe comprises a nucleic acid residue that is a deoxythymidine or uridine residue.
  • An interrogation position of the third probe comprises a nucleic acid residue that is a deoxyguanosine or guanosine residue.
  • An interrogation position of the fourth nucleic acid probe comprises a nucleic acid residue that is a deoxycytosine or cytosine residue.
  • all four probes can be used in a single depolymerization reaction, and their released identifier nucleotides are distinguishable.
  • the sample containing a plurality of target nucleic acid sequences is admixed with a plurality of the nucleic acid probes.
  • Several analytical outputs can be obtained from such multiplexed assays.
  • the analytical output obtained when at least one nucleic acid probes hybridizes with partial complementarity to one target nucleic acid sequence is greater than the analytical output when all of the nucleic acid probes hybridize with total complementarity to their respective nucleic acid target sequences
  • the analytical output obtained when at least one nucleic acid probe hybridizes with partial complementarity to one target nucleic acid sequence is less than the analytical output when all of the nucleic acid probes hybridize with total complementarity to their respective nucleic acid target sequences.
  • the analytical output obtained when at least one nucleic acid probe hybridizes with total complementarity to one nucleic acid target sequence is greater than the analytical output when all of the nucleic acid probes hybridize with partial complementarity to their respective nucleic acid target sequences.
  • the analytical output obtained when at least one nucleic acid probe hybridizes with total complementarity to one target nucleic acid sequence is less than the analytical output when all of the nucleic acid probes hybridize with partial complementarity to their respective nucleic acid target sequences.
  • Yet another embodiment of the invention contemplates a method for determining the presence or absence of a first nucleic acid target in a nucleic acid sample that may contain that target or may contain a substantially identical second target.
  • the second target may have a single base substitution, deletion or addition relative to the first nucleic acid target.
  • This embodiment comprises the following steps. A sample to be assayed is admixed with a plurality of nucleic acid probes under hybridizing conditions to form a hybridization composition.
  • the first and second nucleic acid targets each comprise a region of sequence identity except for at least a single nucleotide at a predetermined position that differs between the targets.
  • Each of the nucleic acid probes is substantially complementary to a nucleic acid target region of sequence identity and comprises at least one identifier nucleotide at an interrogation position.
  • An interrogation position of the probe is aligned with the predetermined position of a target when a target and probe are hybridized.
  • Each probe also includes an identifier nucleotide in the 3 ' -terminal region.
  • the hybridization composition is maintained under hybridizing conditions for a time period sufficient to form a treated sample wherein the nucleotide at the interrogation position of the probe is aligned with the nucleotide at the predetermined position in the region of identity of the target.
  • a treated reaction mixture is formed by admixing the treated sample with a depolymerizing amount of an enzyme whose activity is to release one or more nucleotides from the 3 '-terminus of a hybridized nucleic acid probe.
  • the reaction mixture is maintained under depolymerization conditions for a time period sufficient to permit the enzyme to depolymerize the hybridized nucleic acid and release the identifier nucleotides.
  • An analytical output is obtained by analyzing for the presence or absence of identifier nucleotides released from the 3 ' terminus of the hybridized probe.
  • the analytical output indicates the presence or absence of released identifier nucleotide at the predetermined region, and; thereby, the presence or absence of a corresponding nucleic acid target .
  • the above method is comprised of a first probe and a second probe in the same hybridization composition.
  • the first probe comprises a nucleotide an interrogation position that is complementary to a first nucleic acid target at a predetermined position.
  • the second probe comprises a nucleotide at an interrogation position that is complementary to a second nucleic acid target at a predetermined position.
  • the presence or absence of a third nucleic acid target, which is different from the first and second targets, is assayed for in the same sample that may further contain a fourth target that is substantially identical to the third target.
  • the depolymerizing enzyme whose activity is to release nucleotides, is a template-dependent polymerase, whose activity is to depolymerize hybridized nucleic acid, whose 3 ' -terminal nucleotide is matched, in the 3' to 5 ' direction in the presence of pyrophosphate ions to release one or more nucleotides.
  • the enzyme's activity is to depolymerize hybridized nucleic acid to release identifier nucleotides under depolymerizing conditions.
  • this enzyme depolymerizes hybridized nucleic acids whose bases in the 3 ' - terminal region of the probe are matched with total complementarity to the corresponding bases of the nucleic acid target The enzyme will continue to release properly paired bases from the 3 '-terminal region and will stop at or near the location where the enzyme arrives at a base that is mismatched.
  • the depolymerizing enzyme whose activity is to release nucleotides, exhibits a 3' to 5 ' exonuclease activity in which hybridized nucleic acids having one or more mismatched bases at the 3 ' -terminus of the hybridized probe are depolymerized.
  • the enzyme's activity is to depolymerize hybridized nucleic acid to release nucleotides under depolymerizing conditions.
  • the hybrid may be separated from the free probe prior to enzyme treatment. In some embodiments, an excess of target may be used so that the concentration of free probe in the enzyme reaction is extremely low.
  • the depolymerizing enzyme exhibits a 3' to 5 ' exonuclease activity on a double- stranded DNA substrate having one or more matched bases at the 3' terminus of the hybrid.
  • the enzyme's activity is to depolymerize hybridized nucleic acid to release nucleotides containing a 5 ' phosphate under depolymerizing conditions.
  • the nucleic acid sample to be assayed is obtained from a biological sample that is a solid or liquid.
  • Exemplary solid biological samples include animal tissues such as those obtained by biopsy or post mortem, and plant tissues such as leaves, roots, stems, fruit and seeds.
  • Exemplary liquid samples include body fluids such as sputum, urine, blood, semen and saliva of an animal, or a fluid such as sap or other liquid obtained when plant tissues are cut or plant cells are lysed or crushed.
  • the predetermined nucleic acid target sequence is a microbial or viral nucleic acid and nucleic acid probes comprise sequences complementary to those microbial or viral nucleic acid sequences.
  • the predetermined nucleic acid target sequence is a gene or region of a gene that is useful for genomic typing.
  • exemplary target sequences include the
  • Leiden V mutation a mutant ⁇ -globin gene, the cystic fibrosis-related gene in the region of the delta 508 allele, a mutation in a prothrombin gene, congenital adrenal hyperplasia-associated genes, a translocation that takes place in the region of the jbcr gene along with involvement of a segment of the aJl gene, as well as the loss of heterozygosity of the locus of certain alleles as is found in certain cancers and also allelic trisomy. Genomic typing can also be used to assay plant genomes such as that of rice, soy or maize, and the genomes of microbes such as Campylobacter jejuni , Lis teria , E.
  • thermostable DNA polymerase as a depolymerizing enzyme for determining the presence or absence of a plurality of predetermined nucleic acid target sequences in a nucleic acid sample, and comprises the following steps .
  • a treated sample may contain a plurality of predetermined nucleic acid target sequences hybridized to their respective nucleic acid probes whose 3 '-terminal regions are complementary to their predetermined nucleic acid target sequences and include an identifier nucleotide in the 3 ' -terminal region.
  • a treated depolymerization reaction mixture is formed by admixing a treated sample with a depolymerizing amount of a enzyme whose activity is to release an identifier nucleotide from the 3 ' -terminus of a hybridized nucleic acid probe.
  • the depolymerizing enzyme is thermostable and more preferably, the treated reaction mixture also contains (i) adenosine 5' diphosphate, (ii) pyrophosphate, and (iii) a thermostable nucleoside diphosphate kinase (NDPK) .
  • NDPK thermostable nucleoside diphosphate kinase
  • the time period is also sufficient to permit NDPK enzyme to transfer a phosphate from the released nucleoside triphosphate to added ADP, thereby forming ATP.
  • the presence or absence of a nucleic acid target sequence is determined from the analytical output obtained using ATP.
  • thermostable enzyme for determining the presence or absence of a predetermined nucleic acid target sequence in a nucleic acid sample
  • the treated sample is formed by the following further steps.
  • a hybridization composition is formed by admixing the sample to be assayed with a plurality of nucleic acid probes under hybridizing conditions.
  • the 3 '-terminal region of the nucleic acid probe (i) hybridizes with partial or total complementarity to a nucleic acid target sequence when that sequence is present in the sample, and (ii) includes an identifier nucleotide.
  • a treated sample is formed by maintaining the hybridization composition under hybridizing conditions for a time period sufficient for the predetermined nucleic acid target sequence to hybridize with the nucleic acid probe.
  • the depolymerizing enzyme is from a group of thermophilic DNA polymerases comprising Tne triple mutant DNA polymerase, Trie DNA polymerase. Tag DNA polymerase, Ath DNA polymerase, Tvu DNA polymerase, Bst DNA polymerase, and Tth DNA polymerase.
  • the NDPK is that encoded for by the thermophilic bacteria Pyrococcus furiosis (Pfu)
  • a still further embodiment of the invention contemplates determining the presence or absence of a plurality of nucleic acid target sequences in a nucleic acid sample using a plurality of special nucleic acid probes. These special probes hybridize to the target nucleic acid and are then modified to be able to form a hairpin structure. This embodiment comprises the following steps.
  • a treated sample contains a nucleic acid sample that may include a plurality of nucleic acid target sequences, each having an interrogation position, and each hybridized with its respective nucleic acid probe.
  • the probes are comprised of at least two sections. The first section contains the probe 3 ' -terminal about 10 to about 30 nucleotides. These nucleotides are complementary to the target strand sequence at positions beginning about 1 to about 30 nucleotides downstream of the interrogation position. The second section of the probe is located at the 5 '-terminal region of the probe and contains about 10 to about 20 nucleotides of the target sequence.
  • This sequence spans the region the target from the nucleotide at or just upstream (5') of the interrogation position, to the nucleotide just upstream to where the 3 ' - terminal nucleotide of the probe anneals to the target.
  • An optional third section of the probe from zero to about 50, and preferably about zero to about 20 nucleotides in length and comprising a sequence that does not hybridize with either the first or second section, is located between the first and second sections of the probe.
  • the hybridized probes of the treated sample are extended in a template-dependent manner, as by admixture with dNTPs and a template-dependent polymerase, at least through the interrogation position, thereby forming an extended probe/target hybrid.
  • the length of the probe extension is limited by omission from the extension reaction of a dNTP complementary to a nucleotide of the target sequence that is present upstream of the interrogation position and absent between the nucleotide complementary to the 3 ' -end of the interrogation position.
  • the extended probe/target hybrids are separated from any unreacted dNTPs .
  • the extended probe/target hybrid is denatured to separate the strands .
  • the extended probe strands are permitted to form hairpin structures .
  • a treated reaction mixture is formed by admixing the hairpin structure-containing composition with a depolymerizing amount of an enzyme whose activity is to release one or more nucleotides from the 3 ' -terminus of an extended probe hairpin structure.
  • the reaction mixture is maintained under depolymerizing conditions for a time period sufficient for the depolymerizing enzyme to release 3 ' -terminus nucleotides, and then analyzed for the presence of released identifier nucleotides.
  • the analytical output indicates the presence or absence of the nucleic acid target sequences . In a preferred embodiment, the analytical output for the various targets are distinguishable.
  • a still further embodiment of the invention termed REAPERTM, also utilizes hairpin structures.
  • This method contemplates determining the presence or absence of a plurality of nucleic acid target sequences, or a specific base within a target sequence, in a nucleic acid sample, and comprises the following steps.
  • a treated sample is provided that contains a nucleic acid sample that may include a plurality of nucleic acid target sequences hybridized with their respective first nucleic acid probe strands .
  • the hybrid is termed the first hybrid.
  • the first probes are comprised of at least two sections.
  • the first section contains the probe 3 ' -terminal about 10 to about 30 nucleotides that are complementary to the target nucleic acid sequence at a position beginning about 5 to about 30 nucleotides downstream of the target interrogation position.
  • the second section of the first probe contains about 5 to about 30 nucleotides that are a repeat of the target sequence from the interrogation position to about 10 to about 30 nucleotides downstream of the interrogation position, and does not hybridize to the first section of the probe.
  • An optional third section of the probe, located between the first and second sections of the probe is zero to about 50, preferably up to about 20, nucleotides in length and comprises a sequence that does not hybridize to either the first or second section.
  • the first hybrid in the treated sample is extended at the 3 ! -end of the first probes, thereby extending the first probes past the interrogation position and forming an extended first hybrid whose sequence includes an interrogation position.
  • the extended first hybrid is comprised of the original target nucleic acids and extended first probes.
  • the extended first hybrid is then denatured in an aqueous composition to separate the two nucleic acid strands of the hybridized duplexes and form an aqueous solution containing separated target nucleic acids and a separated extended first probes.
  • Second probes that are about 10 to about 2000, preferably about 10 to about 200, most preferably about 10 to about 30 nucleotides in length and is complementary to the extended first probes at a position beginning about 5 to about 2000, preferably about 5 to about 200, nucleotides downstream of the interrogation position in extended first probe, is annealed to the extended first probe, thereby forming the second hybrid.
  • the second hybrids is extended at the 3 ' -end of the second probes until that extension reaches the 5 ' -end of the extended first probes, thereby forming a second extended hybrid whose 3 ' -region includes an identifier nucleotide.
  • the extending polymerase for both extensions does not add a nucleotide to the 3 ' end that does not have a corresponding complementary nucleotide in the template .
  • An aqueous composition of the extended second hybrid is denatured to separate the two nucleic acid strands.
  • the aqueous composition so formed is cooled to form a "hairpin structure" from the separated extended second probes when its respective target sequence is present in the original nucleic acid sample.
  • a treated reaction mixture is formed by admixing the hairpin structure-containing composition with a depolymerizing amount of an enzyme whose activity is to release one or more nucleotides from the 3 ' -terminus of a nucleic acid hybrid.
  • the reaction mixture is maintained under depolymerizing conditions for a time period sufficient to release 3 ' -terminal region identifier nucleotides, and then analyzed for the presence of released identifier nucleotide.
  • the analytical output indicates the presence or absence of the various nucleic acid target sequences .
  • the present invention has many benefits and advantages, several of which are listed below.
  • One benefit of the invention is that, in some embodiments, a plurality of nucleic acid hybrids can be detected with very high levels of sensitivity without the need for radiochemicals or electrophoresis .
  • An advantage of the invention is that the presence or absence of a plurality of target nucleic acid(s) can be detected reliably, reproducibly, and with great sensitivity.
  • a further benefit of the invention is that quantitative information can be obtained about the amount of a target nucleic acid sequence present in a sample.
  • a further advantage of the invention is that very slight differences in nucleic acid sequence are detectable, including single nucleotide polymorphisms (SNPs) .
  • SNPs single nucleotide polymorphisms
  • Yet another benefit of the invention is that the presence or absence of a number of target nucleic acid sequences can be determined in the same assay.
  • Yet another advantage of the invention is that the presence or absence of target nucleic acids can be determined with a small number of reagents and manipulations .
  • Another benefit of the invention is that the processes lend themselves to automation. Still another benefit of the invention is its flexibility of use in many different types of applications and assays including, but not limited to, detection of mutations, translocations, and SNPs in nucleic acid (including those associated with genetic disease) , determination of viral load, specie ⁇ identification, sample contamination, and analysis of forensic samples.
  • Fig. 1 illustrates the annealing of the 10865 oligonucleotide (SEQ ID NO: 82) to 10870 wild type (SEQ ID NO:83) and 10994 mutant (SEQ ID NO:84) oligonucleotides utilized in rolling circle amplification as Fig. 1A and Fig. IB, respectively.
  • oligonucleotide 10866 to oligonucleotide 10865
  • hybridization to oligonucleotide 10869
  • oligonucleotide probe 10989 SEQ ID NO: 86
  • Arcuate lines in oligonucleotide 10865 are used to help illustrate the shape that oligonucleotide 10865 can assume when hybridized with either of oligonucleotides 10870 or 10994.
  • Fig. 2. illustrates the ReaperTM assay as illustrated in Example 89.
  • Fig. 2A illustrates the first hybrid formed by the annealing of nucleic acid target SEQ ID NO: 61 (61) to first probe SEQ ID NO: 62 (62) .
  • An arrow points to an interrogation position in 286.
  • Fig. 2B illustrates the first extended hybrid formed by the annealing of 61 to the extended 62.
  • Extended 287 is first extended probe SEQ ID NO:
  • Fig. 2C illustrates the second hybrid formed by annealing of 63 from the denatured nucleic acid molecule shown in Fig. 2B to the second probe denoted SEQ ID NO : 64 (64) .
  • An arrow points to the interrogation position in 63.
  • Fig. 2D illustrates the extended second hybrid formed by the annealing of 63 and the extended
  • Fig. 2E illustrates the 65 strand denatured from Fig. 2D and forming a hairpin structure.
  • An arrow points to the interrogation position at the 3 ' - terminus of the hybrid.
  • Nucleoside refers to a compound consisting of a purine [guanine (G) or adenine (A) ] or pyrimidine [thymine (T) , uridine (U) or cytidine (C) ] base covalently linked to a pentose, whereas "nucleotide” refers to a nucleoside phosphorylated at one of its pentose hydroxyl groups.
  • XTP ribonucleotides and deoxyribonucleotides, wherein the "TP” stands for triphosphate, "DP” stands for diphosphate, and "MP” stands for monophosphate, in conformity with standard usage in the art .
  • Subgeneric designations for ribonucleotides are “NMP”, “NDP” or “NTP”
  • subgeneric designations for deoxyribonucleotides are “dNMP", “dNDP” or “dNTP”.
  • dNMP deoxyribonucleotides
  • nucleic acid is a covalently linked sequence of nucleotides in which the 3 ' position of the pentose of one nucleotide is joined by a phosphodiester group to the 5' position of the pentose of the next, and in which the nucleotide residues (bases) are linked in specific sequence; i.e., a linear order of nucleotides.
  • polynucleotide is a nucleic acid containing a sequence that is greater than about 100 nucleotides in length.
  • oligonucleotide is a short polynucleotide or a portion of a polynucleotide.
  • An oligonucleotide typically contains a sequence of about two to about one hundred bases. The word “oligo” is sometimes used in place of the word “oligonucleotide” .
  • a base “position” as used herein refers to the location of a given base or nucleotide residue within a nucleic acid.
  • nucleic acid of interest is any particular nucleic acid one desires to study in a sample.
  • isolated when used in relation to a nucleic acid or protein, refers to a nucleic acid sequence or protein that is identified and separated from at least one contaminant (nucleic acid or protein, respectively) with which it is ordinarily associated in its natural source. Isolated nucleic acid cr protein is present in a form or setting that is different from that in which it is found in nature. In contrast, non-isolated nucleic acids or protems are found in the state they exist in nature.
  • purified or “to purify” means the result of any process which removes some contaminants from the component of interest, such as a protein or nucleic acid. The percent of a purified component is thereby increased in the sample .
  • wild-type refers to a gene or gene product that has the characteristics of that gene or gene product that is most frequently observed in a population and is thus arbitrarily designated the “normal” or “wild-type” form of the gene.
  • modified or mutant refers to a gene or gene product that displays modifications in sequence and/or functional properties (i.e., altered characteristics) when compared to the wild-type gene or gene product .
  • Nucleic acids are known to contain different types of mutations.
  • a "point” mutation refers to an alteration in the sequence of a nucleotide at a single base position.
  • a “lesion”, as used herein, refers to site within a nucleic acid where one or more bases are mutated by deletion or insertion, so that the nucleic acid sequence differs from the wild-type sequence.
  • a "single nucleotide polymorphism” or SNP, as used herein, is a variation from the most frequently occurring base at a particular nucleic acid position.
  • Regions of homologous genes or alleles from different species are also known to vary in sequence. Regions of homologous genes or alleles from different species can be essentially identical in sequence. Such regions are referred to herein as "regions of identity.” It is contemplated herein that a "region of substantial identity" can contain some
  • mismatch position where bases at the same position in the region of identity are different. This base position is referred to herein as “mismatch position.”
  • DNA molecules are said to have a "5'- terminus" (5' end) and a "3 ' -terminus” (3' end) because nucleic acid phosphodiester linkages occur to the 5 ' carbon and 3 ' carbon of the pentose ring of the substituent mononucleotides .
  • the end of a polynucleotide at which a new linkage would be to a 5' carbon is its 5' terminal nucleotide.
  • the end of a polynucleotide at which a new linkage would be to a 3' carbon is its 3' terminal nucleotide.
  • a terminal nucleotide, as used herein, is the nucleotide at the end position of the 3'- or 5 '-terminus.
  • nucleic acid sequence even if internal to a larger oligonucleotide or polynucleotide, also can be said to have 5'- and 3'- ends.
  • a gene sequence located within a larger chromosome sequence can still be said to have a 5 1 - and 3' -end.
  • the 3 ' -terminal region of the nucleic acid probe refers to the region of the probe including nucleotides within about 10 residues from the 3 ' -terminal position.
  • RNA is made by the sequential addition of ribonucleotide-5 ' - triphosphates to the 3 ' -terminus of the growing chain (with the elimination of pyrophosphate) .
  • target nucleic acid or “nucleic acid target” refers to a particular nucleic acid sequence of interest.
  • the “target” can exist in the presence of other nucleic acid molecules or within a larger nucleic acid molecule.
  • nucleic acid probe refers to an oligonucleotide or polynucleotide that is capable of hybridizing to another nucleic acid of interest.
  • a nucleic acid probe may occur naturally as in a purified restriction digest or be produced synthetically, recombinantly or by PCR amplification .
  • nucleic acid probe refers to the oligonucleotide or polynucleotide used in a method of the present invention.
  • oligonucleotide could also be used, for example, in a PCR method as a primer for polymerization, but as used herein, that oligonucleotide would then be referred to as a "primer" .
  • oligonucleotides or polynucleotides may contain some modified linkages such as a phosphorothioate bond.
  • the terms "complementary” or “complementarity” are used in reference to nucleic acids ( i . e . , a sequence of nucleotides) related by the well-known base-pairing rules that A pairs with T and C pairs with G.
  • the sequence 5 ' -A- G-T-3 ' is complementary to the sequence 3'-T-C-A-5'.
  • Complementarity can be “partial,” in which only some of the nucleic acid bases are matched according to the base pairing rules. On the other hand, there may be “complete” or “total” complementarity between the nucleic acid strands when all of the bases are matched according to base pairing rules .
  • the degree of complementarity between nucleic acid strands has significant effects on the efficiency and strength of hybridization between nucleic acid strands as known well in the art. This is of particular importance in detection methods that depend upon binding between nucleic acids, such as those of the invention.
  • the term "substantially complementary” refers to any probe that can hybridize to either or both strands of the target nucleic acid sequence under conditions of iow stringency as described below or, preferably, in polymerase reaction buffer (Promega, M195A) heated to 95°C and then cooled to room temperature.
  • polymerase reaction buffer Promega, M195A
  • hybridization is used in reference to the pairing of complementary nucleic acid strands.
  • Hybridization and the strength of hybridization i.e., the strength of the association between nucleic acid strands
  • the degree of complementarity between the nucleic acids is impacted by many factors well known in the art including the degree of complementarity between the nucleic acids, stringency of the conditions involved affected by such conditions as the concentration of salts, the T m (melting temperature) of the formed hybrid, the presence of other components ( e . g. , the presence or absence of polyethylene glycol) , the molarity of the hybridizing strands and the G:C content of the nucleic acid strands.
  • stringency is used in reference to the conditions of temperature, ionic strength, and the presence of other compounds, under which nucleic acid hybridizations are conducted. With “high stringency” conditions, nucleic acid base pairing will occur only between nucleic acid fragments that have a high frequency of complementary base sequences. Thus, conditions of
  • T m is used in reference to the "melting temperature” .
  • the melting temperature is the temperature at which 50% of a population of double-stranded nucleic acid molecules becomes dissociated into single strands.
  • the equation for calculating the T m of nucleic acids is well-known in the art.
  • homology refers to a degree of complementarity. There can be partial homology or complete homology (i . e . , identity) .
  • a partially complementary sequence that at least partially inhibits a completely complementary sequence from hybridizing to a target nucleic acid is referred to using the functional term "substantially homologous . "
  • the term “substantially homologous”, as used herein, refers to a probe that can hybridize to a strand of the double-stranded nucleic acid sequence under conditions of low stringency.
  • the term “substantially homologous”, as used herein, refers to a probe that can hybridize to (i.e., is the complement of) the single-stranded nucleic acid template sequence under conditions of low stringency.
  • interrogation position refers to the location of a given base of interest within a nucleic acid probe.
  • the "interrogation position" in the probe is in the position that would be complementary to the single nucleotide of the target that may be altered from wild type.
  • the analytical output from a method of the invention provides information about a nucleic acid residue of the target nucleic acid that is complementary to an interrogation position of the probe.
  • An interrogation position is within about ten bases of the actual 3 ' -terminal nucleotide of the nucleic acid probe, although not necessarily at the 3 ' -terminal nucleotide position.
  • the interrogation position of the target nucleic acid sequence is opposite the interrogation position of the probe, when the target and probe nucleic acids are hybridized.
  • identifier nucleotide refers to a nucleotide whose presence is to be detected in a process of the invention to identify that a depolymerization reaction has occurred.
  • the particular application of a method of the invention affects which residues are considered an identifier nucleotide.
  • ATP detection e.g. luciferase/luciferin or NADH
  • all nucleotides released in the depolymerization are "converted" to ATP with an enzyme such as NDPK
  • all nucleotides released are identifier nucleotides.
  • all released nucleotides are identifier nucleotides.
  • all released nucleotides can be identifier nucleotides; alternatively a particular nucleotide
  • a fluorescently-labeled nucleotide is an identifier nucleotide.
  • the nucleotide may be labeled prior to or after release from the nucleic acid.
  • a radioactively- labeled nucleotide is an identifier nucleotide.
  • the release of identifier nucleotide is deduced by analyzing the remainder of the probe after a depolymerization step of the invention. Such analysis is generally by a determination of the size or mass of the remaining probe and can be by any of the described analytical methods (e.g. a fluorescent tag on the 5 '-terminus of the probe to monitor its molecular weight following capillary electrophoresis) .
  • sample is used in its broadest sense.
  • a sample suspected of containing a nucleic acid can comprise a cell, chromosomes isolated from a cell (e.g., a spread of metaphase chromosomes) , genomic DNA, RNA, cDNA and the like.
  • detection refers to quantitatively or qualitatively identifying a nucleotide or nucleic acid within a sample.
  • depolymerization refers to the removal of a nucleotide from the 3' end of a nucleic acid.
  • allele refers to an alternative form of a gene and the term "locus,” as used herein, refers to a particular place on a nucleic acid molecule.
  • a multiplex method of this invention is used to determine the presence or absence of a plurality of predetermined (known) nucleic acid target sequences in a nucleic acid sample.
  • a nucleic acid target is "predetermined” in that its sequence must be known to design a probe that hybridizes with that target.
  • a nucleic acid target sequence as used with respect to a process of this invention can merely act as a reporter to signal the presence of a different nucleic acid whose presence is desired to be determined. That other nucleic acid of interest does not have to have a predetermined sequence .
  • a process of the invention is useful in determining the identity of a base within a target where only enough of the sequence is known to design a probe that hybridizes to that target with partial complementarity at the 3 ' -terminal region of the probe .
  • Such a method utilizes an enzyme that can depolymerize the 3 ' -terminus of an oligonucleotide probe hybridized to the nucleic acid target sequence to release one or more identifier nucleotides whose presence or absence can then be determined as an analytical output that indicates the presence or absence of the target sequence.
  • a nucleic acid target sequence is predetermined in that a nucleic acid probe is provided to be partially or totally complementary to that nucleic acid target sequence.
  • a nucleic acid target sequence is a portion of nucleic acid sample with which the probe hybridizes if that target sequence is present in the sample.
  • a first step of the method is admixing a sample to be assayed with a plurality of nucleic acid probes.
  • the admixing of the first step is typically carried out under low stringency hybridizing conditions to form a hybridization composition.
  • the 3 ' -terminal region of the nucleic acid probes (i) hybridize with partial or total complementarity to a nucleic acid target sequence that may be present in the sample; and (11) include an identifier nucleotide in the 3'- terminal region.
  • a nucleic acid probe is designed to not hybridize with itself to form a hairpin structure in such a way as to interfere with hybridization of the 3 ' -terminal region of the probe to the target nucleic acid.
  • Parameters guiding probe design are well known in the art.
  • the hybridization composition is maintained under hybridizing conditions for a time period sufficient to form a treated sample that may contain a plurality of predetermined nucleic acid target sequences hybridized with their respective nucleic acid probes.
  • the sample to be assayed does not contain a target sequence to which a probe hybridizes, no hybridization takes place for that probe.
  • the resulting treated sample may not contain a substrate for the enzymes of the present invention.
  • a 3' terminal region identifier nucleotide is not released and the analytical output is at or near background levels.
  • the contemplated method is a multiplex assay in which a plurality of probes is utilized to determine whether one or more of a plurality of predetermined nucleic acid target sequences is present or absent in a sample.
  • a particularly useful area for such multiplex assays is in screening assays where the usual analytical output indicates that the sought-after nucleic acid is absent.
  • a nucleic acid sample is screened for the presence of a plurality of predetermined mutant nucleic acid.
  • the mutants usually are not present and the analytical output is, for example, at about background levels except where a mutation is present.
  • a plurality of samples is examined for the presence or absence of microbe- specific nucleic acid.
  • the absence of the sought-after nucleic acid provides an analytical output that is about background levels, and only in the rare instance does a greater than the background output appear.
  • the sample is admixed with a plurality of different nucleic acid probes, preferably after amplification of the multiple nucleic acid targets as needed.
  • the analytical output for a certain result with one of the probes is distinguishable from the analytical output from the opposite result with all of the probes .
  • the ATP produced via NDPK conversion of released nucleotides in the presence of ADP is detected by a luciferase detection system or an NADH detection system.
  • the pyrophosphate transferring step and the phosphate transferring step are performed in a single pot reaction. In other preferred embodiments, if increased sensitivity is required, the ATP molecules can be amplified.
  • information about the presence or absence of a plurality of nucleic acid target sequences is determined using a process of the invention on a single nucleic acid sample, by admixing the sample with a plurality of nucleic acid probes for various nucleic acid targets.
  • the analytical output obtained when at least one of the nucleic acid probes hybridizes with partial complementarity to its target nucleic acid sequence is greater than the analytical output when all of the nucleic acid probes hybridize with total complementarity to their respective nucleic acid target sequences.
  • the enzyme whose activity is to depolymerize hybridized nucleic acid to release nucleotides exhibits a 3 ' —5 ' -exonuclease activity, depolymerizing hybridized nucleic acids having one or more mismatched bases at the 3 ' -terminus of the hybridized probe .
  • the analytical output obtained when at least one of said nucleic acid probes hybridizes with partial complementarity to its target nucleic acid sequence is less than the analytical output when all of the nucleic acid probes hybridize with total complementarity to their respective nucleic acid target sequences.
  • the enzyme whose activity is to depolymerize hybridized nucleic acid to release nucleotides is a template-dependent polymerase.
  • the analytical output obtained when at least one of said nucleic acid probes hybridizes with total complementarity to its nucleic acid target sequence is greater than the analytical output when all of the nucleic acid probes hybridize with partial complementarity to their respective nucleic acid target sequences.
  • the enzyme whose activity is to depolymerize hybridized nucleic acid to release nucleotides is a template-dependent polymerase.
  • the analytical output obtained when at least one of said nucleic acid probes hybridizes with total complementarity to its target nucleic acid sequence is less than the analytical output when all of the nucleic acid probes hybridize with partial complementarity to their respective nucleic acid target sequences.
  • the enzyme whose activity is to depolymerize hybridized nucleic acid to release nucleotides exhibits a 3 ' —»5 ' -exonuclease activity, depolymerizing hybridized nucleic acids having one or more mismatched bases at the 3 ' -terminus of the hybridized probe .
  • the treated sample is admixed with a depolymerizing amount of an enzyme whose activity is to release one or more identifier nucleotides from the 3 ' -terminus of the probe that is hybridized to the nucleic acid target to form a depolymerization reaction mixture.
  • the choice of enzyme used in the process determines if a match or mismatch at the 3'- terminal nucleotide results in release of that 3'- terminal nucleotide. Further information regarding specific enzyme reaction conditions is discussed in detail hereinafter.
  • the depolymerization reaction mixture is maintained under depolymerizing conditions for a time period sufficient to permit the enzyme to depolymerize hybridized nucleic acid and release identifier nucleotides therefrom to form a treated reaction mixture.
  • the presence or absence of released identifier nucleotides is then determined to obtain an analytical output.
  • the analytical output indicates the presence or absence of a nucleic acid target sequence in the sample.
  • Processes of the invention can also be concerned with the degree of hybridization of the target to the 3 ' -terminal region of the probe. Examples hereinafter show that the distinction between a matched and mismatched base becomes less notable as a single mismatch is at a position further upstream from the 3 ' -terminal region position. There is very little discrimination between a match and mismatch when a single mismatch is ten to twelve residues from the 3 ' -terminal nucleotide position, whereas great discrimination is observed when a single mismatch is at the 3' -terminus.
  • the goal is to determine whether a nucleotide at an interrogation position is a match or a mismatch with the target. Better discrimination between match and mismatch at the interrogation position is observed when an intentional mismatch is introduced about 2 to about 10 nucleotides from the interrogation position or preferably about 2 to about 6 nucleotides from the interrogation position.
  • the distinction of the analytical output between matched and mismatched nucleotides when there is more than a single base that is mismatched within the 3 ' -terminal region can be evident even if mismatches are beyond position 10 from the terminus, for example at position 11 and 12 upstream of the 3 ' - terminal nucleotide.
  • the phrases "about 10" and " 3' -terminal region” are used above.
  • the 3'- terminal region therefore comprises the approximately 10 residues from the 3 ' -terminal nucleotide (or 3 ' terminus) position of a nucleic acid.
  • Hybridization conditions can be empirically ascertained for a control sample for various time periods, pH values, temperatures, nucleic acid probe/target combinations and the like. Exemplary maintenance times and conditions are provided in the specific examples hereinafter and typically reflect low stringency hybridization conditions. In practice, once a suitable set of hybridization conditions and maintenance time periods are known for a given set of probes, an assay using those conditions provides the correct result if the nucleic acid target sequence is present . Typical maintenance times are about 5 to about 60 minutes.
  • the enzyme whose activity is to depolymerize hybridized nucleic acid to release nucleotides from the probe 3 '-terminal end is a template-dependent polymerase.
  • the reverse of a polymerase reaction is used to depolymerize a nucleic acid probe, and the identifier nucleotide is released when the 3 ' - terminal nucleotide of the nucleic acid probe hybridizes with total complementarity to its nucleic acid target sequence.
  • a signal confirms the presence of a nucleic acid target sequence that has the sequence sufficiently complementary to the nucleic acid probe to be detected by the process of the invention.
  • an identifier nucleotide is released when the 3 ' - terminal residue of the nucleic acid probe is mismatched and therefore there is only partial complementarity of the 3 ' -terminus of the nucleic acid probe to its nucleic acid target sequence.
  • the hybrid is typically purified from the un-annealed nucleic acid prior to the enzyme reaction, which releases identifier nucleotides.
  • a signal confirms the presence of a nucleic acid target sequence that is not totally complementary to the nucleic acid probe.
  • an identifier nucleotide is released when the 3 '-terminal residue of the nucleic acid probe is matched to the target nucleic acid.
  • a signal confirms the presence of a nucleic acid target that is complementary at the released identifier nucleotide.
  • hybridization and depolymerization can lead to the release of an identifier nucleotide or to little or no release of such a nucleotide, depending upon whether the probe: target hybrid is matched or mismatched at the 3 ' -terminal region. This is also dependent on the type of enzyme used and the type of end, matched or mismatched, that the enzyme requires for depolymerization activity.
  • the magnitude of a contemplated analytical output under defined conditions is dependent upon the amount of released nucleotides. Where an identifier nucleotide is released, an analytical output can be provided that has a value greater than background. Where an identifier nucleotide is not released either because the target sequence was not present in the original sample or because the probe and depolymerizing enzyme chosen do not provide release of a 3 ' -terminal nucleotide when the target is present, or if the match/mismatch state of the 3'- terminal nucleotide did not match that required for the enzyme used to release a 3 ' -terminal nucleotide, the analytical output is substantially at a background level
  • Template-dependent nucleic acid polymerases capable of pyrophosphorolysis include, but are not limited to, DNA polymerase ⁇ , DNA polymerase ⁇ , T4 DNA polymerase, Tag polymerase, Tne polymerase, Tne triple mutant polymerase, Tt polymerase, Tvu polymerase, Ath polymerase, Bst polymerase, E. coli DNA polymerase I, Klenow fragment, Klenow exo minus (exo-), AMV reverse transcriptase, RNA polymerase and MMLV reverse transcriptase.
  • Klenow exo minus (Klenow exo-) or Tne triple mutant polymerase is utilized for DNA pyrophosphorolysis reactions because of their efficient utilization of 5 ' overhanging DNA ends .
  • Klenow exo minus (Klenow exo-) or Tne triple mutant polymerase is utilized for DNA pyrophosphorolysis reactions because of their efficient utilization of 5 ' overhanging DNA ends .
  • reverse of polymerase activity is utilized for DNA pyrophosphorolysis reactions because of their efficient utilization of 5 ' overhanging DNA ends .
  • a preferred substrate is a DNA probe hybridized to a nucleic acid target sequence with total complementarity at its 3 '-terminus, including an identifier residue at the 3 ' -terminal region.
  • a depolymerization reaction can be catalyzed by bacteriophage T4 polymerase in the absence of NTPs depolymerizes a mismatched hybrid.
  • the released nucleotides, XMPs are produced by nuclease digestion.
  • Nuclease digestion can be accomplished by a variety of nucleases that release a nucleotide with a 5' phosphate, including SI nuclease, nuclease BAL 31, mung bean nuclease, exonuclease III and ribonuclease H. Nuclease digestion conditions and buffers are known in the art . Nucleases and buffers for their use are available from commercial sources.
  • the hybridized nucleic acid probe is depolymerized from its 3 ' -terminal nucleotide.
  • the preferred substrate is a nucleic acid probe hybridized to a nucleic acid target sequence with partial complementarity at its 3 ' -terminal region, most preferably with a mismatch at its 3 ' -terminal residue that is an identifier nucleotide .
  • oligonucleotide probes are typically utilized at about 100 ng to about 1 ⁇ g per 20 ⁇ L depolymerization reaction. That amount provides a probe to target weight ratio of about 200:1 to about 1,000:1.
  • nucleic acid polymerase and pyrophosphate (PP ⁇ ) or an analogue thereof are added to a hybridized sample containing from less than about 100 ⁇ g of target nucleic acid, to less than about 10 pg of nucleic acid.
  • Typical target nucleic acids are present at about 1 to about 5 ng in the sample to be assayed, with a target nucleic acid length of about 30 to about 1000 bp being preferred.
  • a depolymerizing enzyme is preferably present in an amount sufficient to depolymerize a hybridized target :probe . That amount can vary with the enzyme used, the depolymerization temperature, the buffer, and the like, as are well-known in the art.
  • thermostable enzymes For a typical reaction carried out in a 20 ⁇ L volume, about 0.25 to about 1 unit (U) of an enzyme such as Klenow exo- is used. About 1 to about 5 U of the thermostable enzymes are used for depolymerization at elevated temperatures. Other conditions affecting the depolymerization reactions are discussed in the parent applications cited hereinabove, which are incorporated by reference.
  • the analytical output is obtained by detection of the released identifier products, either the released nucleotides or the remainder of the probe.
  • Exemplary detection systems include the light emitting luciferase detection system, the NADH light adsorption detection system (NADH detection system) , fluorescence emissions and mass spectrometry. These detection systems are discussed hereinbelow.
  • nucleotides were released can be deduced through examination of the probe after depolymerization.
  • the determination of the size of an oligonucleotide is well known in the art. For example gel separation and chromatographic separations are well known. Gel imaging techniques that take advantage of fluorescence and absorbance spectroscopy as well as radiographic methods. Mass spectrometry of oligonucleotides is also becoming more common . As is illustrated in the Examples that follow, it can be beneficial to carry out a contemplated method at elevated temperatures, e.g., about 50°C to about 90°C.
  • Tne triple mutant DNA polymerase is described in detail in WO 96/41014, whose disclosures are incorporated by reference, and its 610 residue amino acid sequence is provided as SEQ ID NO: 35 of that document. That enzyme is referred to in WO 96/41014 as Tne M284 (D323A, D389A) . Briefly, that enzyme is a triple mutant of the polymerase encoded by the thermophilic eubacterium Thermotoga neapoli tana. (ATCC 49049) . The amino-terminal 283 residues of the native sequence are deleted and the aspartic acid residues at positions 323 and 389 of the native sequence are replaced by alanine residues in this recombinant enzyme. This recombinant enzyme is thus a deletion and replacement mutant of the native enzyme.
  • Luciferase detection systems are particularly useful for detecting ATP.
  • luciferase catalyzes the oxidation of luciferin, producing light that can then be quantified using a luminometer. Additional products of the reaction are AMP, pyrophosphate and oxyluciferin .
  • ATP detection buffer referred to as L/L reagent (Promega, FF2021) is utilized.
  • L/L reagent Promega, FF2021
  • luciferase a luciferase a luciferase a luciferase a luciferase a luciferase a luciferase a luciferase a luciferase.
  • L/L reagent Promega, FF2021
  • luciferase ase are used in the reaction.
  • the present invention be limited to a specific concentration of luciferase, greater amounts of luciferase have a tendency to increase non-specific background.
  • the dNTPs or NTPs produced by pyrophosphorolysis or nuclease digestion are converted to XTP, which can then be used directly as substrate for luciferase, permitting detection of the nucleic acid.
  • the preferred substrate for luciferase is ATP, as demonstrated by Moyer and
  • NDPK nucleoside diphosphate kinases
  • NTPs or dNTPs to ATP by NDPK is preferably accomplished by adding NDPK and a molar excess of ADP over the amounts of NTPs or dNTPs expected to be produced by pyrophosphorolysis or nuclease digestion, followed by pyrophosphorylation by PRPP synthetase.
  • the utilization of ADP requires optimization of the amount of ADP added. Too much ADP results in high background levels.
  • NDPK (EC 2.7.4.6) preparations from several biological sources are commercially available from several suppliers. For example yeast NDPK is available from Sigma Chemical Co., St. Louis, MO, whereas bovine NDPK is available from ICN Biochemicals, Inc., Costa Mesa, CA.
  • thermostable NDPK such as the Pfu NDPK
  • a thermostable depolymerizing enzyme such as the Tne triple mutant DNA polymerase (discussed below) , Bst DNA polymerase, Ath DNA polymerase, Tag DNA polymerase and Tvu DNA polymerase along with a reaction temperature of about 50°C to about 90°C.
  • Tne triple mutant DNA polymerase is described in detail in WO 96/41014, whose disclosures are incorporated by reference, and its 610 residue amino acid sequence is provided as SEQ ID NO: 35 of that document. That enzyme is referred to in WO 96/41014 as Tne M284 (D323A, D389A) .
  • the presence of released nucleotides is analyzed via mass spectrometry.
  • the treated reaction mixture is ionized in a manner such that all components of the treated reaction mixture in the molecular weight range of the released identifier nucleotides are measured.
  • Very small differences in molecular weight can be detected using mass spectrographic methods (different isotopes of the same atom are detectable) , so any variation from a natural nucleic acid, including a single atom substitution (e.g. a fluorine in place of a hydrogen atom or a replacement of a hydrogen by a deuterium atom) in the identifier nucleotide gives rise to a detectable difference.
  • Nucleic acid analogs used in methods of the invention should not interfere with either the hybridization of the nucleic acid probe or depolymerization of the hybridized probe .
  • mass spectrometry can discriminate between individual nucleotides or nucleosides .
  • mass spectrometry can be used to detect the release of that G nucleotide in a method of the present invention.
  • mass spectrometry can detect the release of an A, T or C nucleotide, based on the differences in atomic weight of these compounds.
  • mass spectrometry can be used to resolve the presence of one or more of these 3'- identifier nucleotides.
  • a mass spectral technique referred to as DIOS desorption/ionization on silicon
  • DIOS desorption/ionization on silicon
  • MALDI mass spectrographic assay techniques
  • multiple different identifier nucleotides can be used in the various nucleic acid probes. Using such a technique the presence of the different identifier nucleotides is direct evidence of the presence of the nucleic acid target sequences.
  • an identifier nucleotide includes a fluorescent label .
  • An identifier nucleotide can be fluorescently labeled prior to, or after, release of the identifier nucleotide.
  • the analytical output is obtained by mass spectrometry.
  • the fluorescent label is part of a fluorescent analog of a nucleotide.
  • Fluorescent nucleotide analogs are widely known and commercially available from several sources.
  • An exemplary source is NENTM Life Science Products (Boston, Massachusetts), who offer dideoxy- , deoxy- , and ribonucleotide analogs a labeled with fluorescein, coumarin, tetramethylrhodamine, naphthofluorescein, pyrene, Texas Red ® , and
  • LissamineTM LissamineTM. Other suppliers include Amersham Pharmacia Biotech (Uppsala, Sweden; Piscataway, New Jersey) and MBI Fermentas, Inc. (Amherst, New York) .
  • An advantage to using fluorescent labels and fluorescence spectroscopy analysis is that there are multiple different labels. Such different labels would be particularly useful in a multiplex embodiment of the invention. Different fluorescent labels would be used in different probes, so that the detection of a particular fluorescently-labeled nucleotide analog as a released identifier nucleotide could be used to deduce which nucleic acid targets are present .
  • fluorescein has a 488 nm excitation and 520 nm emission wavelength
  • rhodamine in the form of tetramethyl rhodamine
  • a fluorescence detector provides an excitation source and an emission detector. The emission wavelengths of 520 nm and 575 nm are easily distinguishable using fluorescence spectroscopy.
  • fluorescence spectroscopy On a per molecule basis, fluorescence spectroscopy is about 10 -fold more sensitive than absorbance spectroscopy.
  • a very wide variety of fluorescence spectroscopy-based detectors are commercially available for reading fluorescence values of single tubes, flow cells and multi-well plates, among others.
  • Labsystems Multiskan models of microplate readers are widely available with a spectral range of 400 to 750 nm, and filters for 340, 405, 414, 450, 492, 540, 620, and 690 nm (e.g. Fisher Scientific, Pittsburgh, Pennsylvania) .
  • a released identifier nucleotide could be labeled before or after depolymerization using cross-linking chemistry well known in the art with commercially available reagents.
  • fluorescein isothiocyanate and rhodamine B isothiocyanate are both available from Aldrich Chemical Company (Milwaukee, Wisconsin) .
  • References to fluorescein isothiocyanate ' s use in labeling biological molecules include Nature, 193:167 (1962), Methods Enzymol . 26:28 (1972), Anal. Biochem . , 57:227 (1974), Proc . Na tl . Acad . Sci . , U. S .
  • NADH detection system a combination of two enzymes, phosphoglycerate kinase and glyceraldehyde phosphate dehydrogenase, is used to catalyze the formation of NAD from NADH in the presence of ATP. Because NADH is fluorescent whereas NAD is not, ATP is measured as a loss in fluorescence intensity. Examples of NADH based ATP assays are disclosed in United States Patent Nos. 4,735,897, 4,595,655, 4,446,231 and 4,743,561, and UK Patent Application GB 2,055,200, all of which are herein incorporated by reference.
  • An absorbance spectrographic analysis step is contemplated to provide an analytical output, thereby provide for the determination of the presence or absence released identifier nucleotide, and indicate the presence or absence of said nucleic acid target sequence.
  • This embodiment contemplates the chromatographic separation of a reaction mixture that has been treated with a depolymerizing amount of an enzyme whose activity is to release one or more nucleotides from the 3' -terminus of a hybridized nucleic acid.
  • a multiplexed assay for the presence of several different nucleic acid target sequences in a sample is analyzed by absorbance spectroscopy.
  • Several labeled probes to various nucleic acid target sequences are added to a nucleic acid sample .
  • the labels on the probes may be various nucleotide analogs, a different one for each probe.
  • a depolymerizing enzyme is added, such as Klenow exo-, releasing the labeled nucleotides and other nucleotides from the 3 '-termini of probes hybridized to target sequences when the 3 ' terminal nucleotide is matched.
  • reaction solution is loaded onto a pre- equilibrated High Pressure Liquid Chromatography (HPLC) column and eluted under conditions that separate the nucleotide analogs from the natural nucleotides.
  • HPLC High Pressure Liquid Chromatography
  • Useful media for chromatographic separation of nucleotides, bases, and nucleosides include reverse phase media, such as a reverse phase C18 column or ODS-80T M or ODS-120T TSK-GEL by TosoHaas (Montgomeryville, Pennsylvania), anion exchange media, such as DEAE-25SW or SP-25W TSK-GEL by
  • Example 5 illustrates an embodiment of the present invention using HPLC.
  • the HPLC column is fitted with an absorbance detector to monitor the column effluent.
  • absorbance spectroscopy for this type of analysis.
  • Typical wavelengths for monitoring HPLC detection of nucleotides are 250 nm, 260 nm and 280 nm.
  • Such separations of nucleotides and nucleotide analogs are well known in the art. Revich et al . , J. Chromatography, 317:283-300 (1984), and Perrone & Brown, J " . Chromatography, 317:301-310 (1984) provide examples of the HPLC separation of dNTPs.
  • Identification of the separated nucleotide analogs can be accomplished by comparison of the retention times (as monitored by absorbance of effluent at various times) of standards of the nucleotide analogs separated on the same HPLC column under the same conditions.
  • identity of the nucleotide analogs collected in separate fractions can be determined by other standard analytical methods, such as nuclear magnetic resonance or atomic analysis (H,C,N) .
  • the presence of a released identifier nucleotide from a particular probe indicates the presence of the target sequence that hybridize with that probe.
  • the released nucleotides from a depolymerization reaction mixture are separated on a gas chromatograph fitted with an absorbance detector to monitor column effluent.
  • Depolymerization reactions can be used to interrogate the identity of a specific base in a nucleic acid.
  • identity of single base point mutations, deletions, or insertions in a nucleic acid can be determined as follows.
  • each nucleic acid probe synthesized is substantially complementary to a target nucleic acid containing or suspected of containing a point mutation. It will be recognized that various hybridization conditions can be used, so as to vary the stringency at which hybridization occurs. Thus, depending upon the system utilized, the complementarity of the probe can be varied.
  • the probe can have as many as 10 base mismatches with the target nucleic acid, and preferably less than 5 mismatches. Most preferably, the probe has only one base mismatch with the target nucleic acid or is completely complementary to the target nucleic acid.
  • a nucleic acid probe comprises single- stranded nucleic acid (e . g. , DNA or RNA) .
  • a probe can be of varying lengths, preferably from about 10 to 100 bases, most preferably about 10 to 30 bases.
  • a probe is complementary to the target at all bases between an interrogation position and 3 ' end of the nucleic acid probe .
  • a probe is designed to have a predetermined nucleotide at an interrogation position. When a complementary probe base pairs or hybridizes to a target nucleic acid, the base at an interrogation position aligns with the base in the nucleic acid target whose identity is to be determined under conditions such that base pairing can occur.
  • an interrogation position can be varied within the probe.
  • an interrogation position is preferably within 10 bases of the 3' end of the nucleic acid probe.
  • an interrogation position is within 6 bases of the 3 ' end of the nucleic acid probe.
  • an interrogation position is at the next to last or last base at the 3 ' end of the nucleic acid probe.
  • a set of DNA probes includes a first probe with a deoxyadenosine residue at an interrogation position, a second probe with a deoxythymidine residue at an interrogation position, a third probe with a deoxyguanosine residue at an interrogation position, and a fourth probe with a deoxycytosine residue at an interrogation position.
  • a set of RNA probes includes a first probe with an adenosine residue at an interrogation position, a second probe with a uridine residue at an interrogation position, a third probe with a guanosine residue at an interrogation position, and a fourth probe with a cytosine residue at an interrogation position.
  • the probes are hybridized to the target nucleic acid, if the target nucleic acid is present in the sample, so that a probe nucleic acid-target nucleic acid complex is formed. It is contemplated that hybridization conditions can vary depending on the length and base composition of the probes.
  • the nucleotide at an interrogation position is aligned with the specific base to be identified in the nucleic acid.
  • a set of probes can be used simultaneously. Because the probes differ at an interrogation position, only one of the probes is complementary to the specific base in the target nucleic acid that is aligned with an interrogation position.
  • the probes are distinguishable, most preferably the identifier nucleotides are different between the four probes, for example using mass spectrometry or different fluorescent labels.
  • the nucleic acid probe-target nucleic acid complexes are reacted under conditions permitting depolymerization of the probe.
  • the preferred reaction conditions for depolymerization are described in the parent applications and in the following Examples.
  • the released nucleotides are then detected.
  • the identity of a specific base is determined by comparing the amount of signal produced from each probe. Depolymerization of a hybridized probe proceeds from its 3' end. When the base at an interrogation position is not complementary to the specific base in the nucleic acid, very little or no signal is produced.
  • the probe-mediated specific nucleic acid detection method of the present invention can be used to simply identify or detect a nucleic acid of interest.
  • nucleic acid probes e . g. , DNA or RNA
  • each nucleic acid probe is entirely complementary to its target nucleic acid.
  • a nucleic acid probe comprises single-stranded nucleic acid (e.g., DNA or RNA) .
  • the probe can be of varying lengths, preferably from about 10 to about 1000 bases, most preferably about 10 to 100 bases.
  • Detection is carried out as described above.
  • the nucleic acid probe-nucleic acid target complex is exposed to conditions permitting depolymerization of the probe, which results in the production of XTPs .
  • Detection of the nucleic acid of interest is characterized by a difference in the signal generated by the XTPs produced when compared to control sample reactions.
  • a signal greater than background would indicate the presence of at least one of the target nucleic acids in the original sample.
  • each probe contains a distinguishing identifier nucleotide and the detection of an identifier nucleotide released from the target/probe hybrid would determine the presence of a specific target nucleic acid in the original sample.
  • the ability to interrogate the identity of a specific base in a nucleic acid also permits discrimination between nucleic acids from different species, or even from different alleles.
  • the ability to detect and discriminate between nucleic acids of related or unrelated species also permits the identification of species contained within a given nucleic acid-containing sample.
  • the method can be used to determine which species of several related bacteria or virus are contained within a sample ( e . g. , clinical samples, environmental samples, food samples, or samples from non-human animals) .
  • nucleic acids with substantially identical sequences from at least two species or alleles are detected.
  • the region of identity contains at least a single nucleotide mismatch between the species or alleles in at least one predetermined position and also contains a 3 ! end and a 5' end or the identification of a nucleic acid sequence unique to each species to be identified.
  • an RNA or DNA probe that is substantially complementary to the region of identity is synthesized.
  • the probe can be of varying lengths, preferably from about 10 to 1000 bases, most preferably about 10 to 100 bases. As above, this complementary probe includes an interrogation position.
  • An interrogation position can be varied within the probe.
  • an interrogation position is preferably within 10 bases of the 3' end of the nucleic acid probe. More preferably, an interrogation position is within 6 bases of the 3 ' end of the nucleic acid probe. Most preferably, an interrogation position is at the next to last or last base of the 3' end of the nucleic acid probe.
  • the nucleic acid probes are designed so that the base at an interrogation position is complementary to the nucleotide at the predetermined position of one species or allele, but not another due to the mismatch.
  • a second probe can be synthesized that is complementary at an interrogation position to the nucleotide at the predetermined position of a second species or allele.
  • a contemplated procedure is employed to identify the presence or absence of multiple species within a given sample. In these embodiments, all that is required is the identification of substantially identical sequences between species that contain base mismatches or the identification of a nucleic acid sequence unique to each species to be identified.
  • a method contemplated by the present invention has wide applicability in assaying nucleic acids.
  • an endogenous nucleic acid is assayed to determine whether a particular native or mutant sequence is present or absent. This type of analysis is sometimes referred to as genotyping because the genetic makeup of the subject from which the nucleic acid sample is obtained is determined.
  • genotyping because the genetic makeup of the subject from which the nucleic acid sample is obtained is determined.
  • the identity of an organism such as the identification of a human, dog, chicken, bovine or the like can be determined by use of species-specific nucleic acid probes such as probes to selected regions of the gene encoding cytochrome B .
  • a human patient for example, has the Leiden V mutation, a mutant ⁇ -globin gene, the cystic fibrosis-related gene in the region of the delta 508 allele, a mutation in a prothrombin gene, congenital adrenal hyperplasia, a translocation that takes place in the region of the jbcr gene along with involvement of a segment of the abl gene, the number of repeated sequences in a gene such as are present in THO 1 alleles or the TPOX alleles, as well as the loss of heterozygosity of the locus of certain alleles as is found in certain cancers and also allelic trisomy.
  • Genomic typing can also be used to assay plant genomes such as that of rice, soy or maize to determine if they contain non-native sequences.
  • the presence or absence in a sample of the genomes of microbes such as Campylobacter jejuni , Listeria , and E. coli 0H157 can be determined, and viral genomes such as that of cytomegalovirus (CMV) or human immunodeficiency virus (HIV) can be analyzed to determine whether a drug-resistant strain is present in a sample .
  • CMV cytomegalovirus
  • HMV human immunodeficiency virus
  • a contemplated method can also be utilized to assay for the presence or absence of nucleic acid that is exogenous to the source of the sample.
  • a contemplated method can be used to assay for the presence of viruses such as hepatitis C virus (HCV) , cytomegalovirus (CMV) , human immunodeficiency virus (HIV) , as well as to determine the viral load in an organism with a disease, such as a human or a plant .
  • viruses such as hepatitis C virus (HCV) , cytomegalovirus (CMV) , human immunodeficiency virus (HIV)
  • a contemplated method can also be used to identify the presence of an exogenous nucleic acid sequence in a plant such as maize, soy or rice.
  • a contemplated method can also be used to assay for the presence of microorganisms such as Listeria monocytogenes , Campylobacter spp . , Salmonella spp . , Shigella spp . or Escherichia coli (including E. coli E0157) in foodstuffs such as meats
  • nucleic acid target sequence useful for designing nucleic acid probes for use in a method of the invention is within the skill of the art.
  • Databases of genetic sequences such as Genbank, can be used to ascertain the uniqueness of the selected nucleic acid target .
  • Commercially available software for designing PCR primers can be used to assist in the design of probes for use in the invention.
  • the predetermined nucleic acid target sequences are associated with blood coagulation
  • nucleic acid probes comprise sequences complementary to nucleic acid sequences associated with blood coagulation.
  • Exemplary sequences associated with blood coagulation comprise (a) a sequence of at least ten nucleotides of the Factor V gene in the region of the Leiden mutation or the corresponding wild type sequence of the Factor V gene; and (b) a sequence of at least ten nucleotides of a prothrombin gene.
  • Preferred exemplary sequences are selected from the group consisting of SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 87, SEQ ID NO: 88, SEQ ID NO: 89, SEQ ID NO: 90, SEQ ID NO: 91, SEQ ID NO: 92, SEQ ID NO: 93, SEQ ID NO: 94, SEQ ID NO: 47, SEQ ID NO: 44, SEQ ID NO: 45 and SEQ ID NO: 46 and their complementary sequences.
  • the speciation of a nucleic acid sample is determined using a suite of species probes in a single assay. Kits containing probes for such an assay are also contemplated. Exemplary probes shown to be specific for human mitochondrial DNA are SEQ ID NO: 50)) and 11583 (SEQ ID NO:51)) . An exemplary common probe,
  • 11582 (SEQ ID NO:52), gives a positive reaction with bovine, chicken, dog and human species.
  • An exemplary chicken-specific probe, 11577 (SEQ ID NO:53), is specific for chicken mitochondrial DNA, while another chicken-specific probe, 11584 (SEQ ID NO:54), gives a signal with bovine and human in addition to chicken genomic DNA.
  • An exemplary cow-specific probe, 11588 (SEQ ID NO: 55) , provides a strong signal with cow target DNA, but also gives a signal with human, chicken and dog nucleic acid.
  • An exemplary dog- specific probe, 11586 (SEQ ID NO:56), provides a stronger signal with dog DNA than it does with cow DNA.
  • the sequences complementary to the probes listed below are also contemplated as probe sequences .
  • genetic screening for a target sequence in a nucleic acid sample is contemplated using a plurality of probes to the various targets in a single assay. Kits containing probes for such genetic testing are also contemplated.
  • the steroid 21-hydroxylase gene is screened for mutations correlated with a group of autosomal recessive diseases collectively known as congenital adrenal hyperplasia (CAH) .
  • CAH congenital adrenal hyperplasia
  • Exemplary CAH probes for use in a method and kit according to the invention are listed below.
  • the complementary sequences to the probes listed below are also contemplated as probe sequences.
  • CAH interrogator oligo 6 wild type for mutation site 1 11085 5' CACCCTCCAGCCCCCAGC 3' SEQ ID NO: 24
  • CAH interrogator oligo 2 (pseudogene/mutant) for mutation site 2
  • CAH interrogator oligo 1 (pseudogene/mutant) for mutation site 1
  • CAH interrogator oligo 9 wild type for mutation site 4 11088 5' GATTCAGCAGCGACTGTA 3' SEQ ID NO: 31
  • CAH interrogator oligo 5 (pseudogene/mutant) for mutation site 5
  • a segment of nucleic acid from the genome or mitochondrial nucleic acid is amplified or otherwise isolated to make a sample for conducting a hybridization assay according to the invention.
  • a method of the invention that results in multiple depolymerizable hybrids in the presence of a single target molecule as discussed in the copending application U.S. Serial No. 09/358,972, filed on July 21, 1999, is preferred, for example assays forming hairpins (e.g. REAPERTM), or using self -annealing primers.
  • This application is a continuation- in-part of U.S. patent application Serial No. 09/358,972, the disclosures of which are incorporated herein by reference and published on the internet at http : //ww . promega . com/pt/pend/09358972. pdf .
  • predetermined nucleic acid target sequences are associated with cystic fibrosis
  • the nucleic acid probes comprise sequences complementary to nucleic acid sequences associated with cystic fibrosis.
  • the target and probes are associated with the cystic fibrosis delta F508 mutation.
  • Particularly preferred exemplary cystic fibrosis- associated sequences are SEQ ID NO: 95 or SEQ ID NO: 96 and their complementary sequences.
  • the nucleic acid probes BA3 (SEQ ID NO: 97) and BA4 (SEQ ID NO: 98) are useful in detecting a particular translocation that takes place in the region of the Jbcr gene , and a segment of the abl gene that is involved with the translocation.
  • a target nucleic acid sequence is typically amplified prior to use of a contemplated method. However, where a sufficient number of repeated nucleotide sequences are present in the native sample as in the human Alu sequence or the E. coli rep sequence, amplification is often not needed prior to carrying out a contemplated method.
  • a claimed process contemplates prior treatment of a nucleic acid sample using any amplification method known in the art at the time of practicing a claimed process to detect the presence of a nucleic acid target in the sample .
  • probes be constructed to be free of hairpin structures
  • assays in which hairpin structures are constructed are also useful.
  • An embodiment of the invention contemplates use of a hairpin structure for determining the presence or absence of a plurality of nucleic acid target sequences in a nucleic acid sample with a probe that is hybridized to the target and then modified to be able to form a hairpin structure. This embodiment comprises the following steps.
  • a treated sample contains a nucleic acid sample that may include a plurality of nucleic acid target sequences having an interrogation position.
  • the target sequences if present in the nucleic acid sample hybridize with their respective nucleic acid probes.
  • a probe is comprised of at least two sections. The first section contains the probe 3 ' -terminal about 10 to about 30 nucleotides. These nucleotides are complementary to the target strand sequence at positions beginning about 1 to about 30 nucleotides downstream of the interrogation position.
  • the second section of the probe is located at the 5 ' -terminal region of the probe and contains about 10 to about 20 nucleotides of the target sequence.
  • This same sequence therefore, exists in both the target and the probe in the same 5 ' to 3 ' orientation.
  • This sequence spans the region in the target from the nucleotide at or just upstream (5') of the interrogation position, to the nucleotide just upstream to where the 3 ' -terminal nucleotide of the probe anneals to the target.
  • An optional third section of the probe from zero to about 50, preferably from zero to about 20, nucleotides in length and comprising a sequence that does not hybridize with either the first or second section, is located between the first and second sections of the probe .
  • the hybridized probes of the treated sample are extended in a template-dependent manner, by admixture with dNTPs and a template-dependent polymerase, at least through the interrogation position, thereby forming an extended probe/target hybrid.
  • the length of the probe extension is limited by omission from the extension reaction of a dNTP complementary to a nucleotide of the target sequence that is present upstream of the interrogation position and absent between the nucleotide complementary to the 3 ' -end of the interrogation position.
  • the extended probe/target hybrid is separated from any unreacted dNTPs; i.e., purified at least to the degree needed to use the extended probe strand to determine the presence or absence of the interrogation region in the sample or the identity of the base at the interrogation position.
  • the extended probe/target hybrid is denatured to separate the strands .
  • the extended probe strands are permitted to form hairpin structures .
  • the polymerase enzyme utilized for an extension reaction be a template- dependent polymerase that is free of activity that adds a 3 ' -terminal deoxyadenosine in a template- nonspecific manner.
  • a polymerase such as Tag
  • a treated reaction mixture is formed by admixing the hairpin structure-containing composition with a depolymerizing amount of an enzyme whose activity is to release one or more nucleotides from the 3 ' -terminus of an extended probe hairpin structure.
  • the reaction mixture is maintained under depolymerizing conditions for a time period sufficient for the depolymerizing enzyme to release 3 ' -terminus nucleotides, and then analyzed for the presence of released identifier nucleotides.
  • the analytical output indicates the presence or absence of the nucleic acid target sequence. That analytical output can be determined as discussed elsewhere herein.
  • a still further embodiment of the invention such as that termed REAPERTM and demonstrated in Example 89 and Figure 2, also contemplates use of hairpin structures in determining the presence or absence of a nucleic acid target sequence, or a specific base within the target sequence, in a nucleic acid sample, and comprises the following steps.
  • a treated sample is provided that contains a nucleic acid sample that may include a plurality of nucleic acid target sequences hybridized with its respective first nucleic acid probe strand (Fig. 2A) .
  • the hybrid is termed the first hybrid.
  • the first probes are comprised of at least two sections.
  • the first section contains the probe 3 ' -terminal about 10 to about 30 nucleotides that are complementary to the target nucleic acid sequence at a position beginning about 5 to about 30 nucleotides downstream of the target interrogation position.
  • the second section of a first probe contains about 5 to about 30 nucleotides that are a repeat of the target sequence from the interrogation position to about 10 to about 30 nucleotides downstream of the interrogation position, and does not hybridize to the first section of the probe. That is, the second sequence is a repeat of the region in the target sequence from the interrogation position downstream to the position where the 3 ' -terminal nucleotide of the first probe aligns with the target.
  • An optional third section of the probe, located between the first and second sections of the probe is zero to about 50, preferably to about 20, nucleotides in length and comprises a sequence that does not hybridize to either the first or second section.
  • the first hybrid in the treated sample is extended at the 3 ' -end of the first probes, thereby extending the first probe past the interrogation position and forming an extended first hybrid (Fig. 2B) whose sequence includes an interrogation position.
  • the extended first hybrid is comprised of the original target nucleic acid and extended first probe.
  • the extended first hybrid is then denatured in an aqueous composition to separate the two nucleic acid strands of the hybridized duplex and form an aqueous solution containing separated target nucleic acids and separated extended first probes.
  • Second probes are about 10 to about 2000, more preferably about 10 to about 200, most preferably about 10 to about 30 nucleotides in length and are complementary to their respective extended first probes at a position beginning about 5 to about 2000, preferably about 5 to about 200, nucleotides downstream of the interrogation position in extended first probe, anneal to the extended first probes, thereby forming the second hybrid (Fig. 2C) .
  • the second hybrid is extended at the 3 ' -end of the second probes until that extension reaches the 5 ' -end of the extended first probes, thereby forming a second extended hybrid (Fig. 2D) whose 3 ' -region includes an identifier nucleotide.
  • An aqueous composition of the extended second hybrid is denatured to separate the two nucleic acid strands; i.e., the extended second probes and the extended first probes.
  • the aqueous composition so formed is cooled to form a "hairpin structure" from the separated extended second probes (Fig. 2E) when the target sequence is present in the original nucleic acid sample.
  • the 3 ' -terminal sequence of the second extended probes in the second extended hybridize with the sequence of the second extended probes from a region comprising the interrogation position and nucleotides downstream from the interrogation position of second extended probe to the nucleotide position where the 3 ' -terminal nucleotide of the original (first-named) probes annealed to the original target .
  • a treated reaction mixture is formed by admixing the hairpin structure-containing composition with a depolymerizing amount of an enzyme whose activity is to release one or more nucleotides from the 3 ' -terminus of a nucleic acid hybrid.
  • the reaction mixture is maintained under depolymerizing conditions for a time period sufficient to release 3 ' -terminal region identifier nucleotides, and then analyzed for the presence of released identifier nucleotides.
  • the analytical output indicates the presence or absence of the various nucleic acid target sequences. Again, the analytical output can be determined by one of the several methods discussed elsewhere herein. In one embodiment of this multiplex hairpin- forming probe method, the analytical outputs from the various nucleic acid target sequences are distinguishable.
  • dNTPs are utilized in the extension reactions. It is preferred that the hairpin structures be separated from the dNTPs prior to depolymerization to enhance the analysis for the identifier nucleotide.
  • kits for determining the presence or absence of a plurality of predetermined nucleic acid target sequences in a nucleic acid sample comprises an enzyme whose activity is to release one or more nucleotides from the 3' terminus of a hybridized nucleic acid probe and at least one nucleic acid probe, said nucleic acid probe being complementary to a nucleic acid target sequence.
  • the enzyme whose activity is to release nucleotides in the kit is a template dependent polymerase that, in the presence of pyrophosphate ions, depolymerizes hybridized nucleic acids whose bases in the 3' -terminal region are matched with total complementarity.
  • the enzyme whose activity is to release nucleotides in the kit exhibits a 3' to 5 ' exonuclease activity, depolymerizing hybridized nucleic acids having one or more mismatched bases at the 3 ' terminus of the hybridized probe.
  • the enzyme capable of catalyzing pyrophosphorolysis is, but is not limited to Tag polymerase, Tne polymerase, Tne triple mutant polymerase, Tth polymerase, Tvu polymerase, Ath polymerase, T4 DNA polymerase, Klenow fragment, Klenow exo minus, E. coli DNA polymerase I, AMV reverse transcriptase, MMLV reverse transcriptase, or poly (A) polymerase.
  • the kit contains an exonuclease such as SI nuclease, nuclease BAL 31, mung bean nuclease, exonuclease III and ribonuclease H.
  • Either of the above enzyme types is utilized in a contemplated method in a depolymerizing effective amount. That is, the enzyme is used in an amount that depolymerizes the hybridized probe to release an identifier nucleotide. This amount can vary with the enzyme used and also with the temperature at which depolymerization is carried out .
  • An enzyme of a kit is typically present in an amount that conveniently permits the distribution of about 0.1 to 100 U per reaction; in particularly preferred embodiments, the concentration is about 0.5 U/reaction.
  • An amount of enzyme sufficient to carry out at least one assay, with its controls is provided.
  • the enzyme whose activity in the presence of pyrophosphate is to release identifier nucleotides is a thermostable polymerase.
  • Preferred thermostable polymerases are the Tne triple mutant DNA polymerase,
  • Klenow exo-, Klenow, T4 DNA polymerase, Ath DNA polymerase, Tag DNA polymerase and Tvu DNA polymerase, the Tne triple mutant DNA polymerase and Tvu DNA polymerase are particularly preferred.
  • kit is useful for any of the methods of the present invention.
  • the choice of particular components is dependent upon the particular method the kit is designed to carry out. Additional components can be provided for detection of the analytical output, as measured by the release of identifier nucleotide, or by detection of the remaining probe after depolymerization.
  • a kit has nucleic acid probes that comprise fluorescent labels.
  • either the released identifier nucleotide or the remaining probe is determined using fluorescence spectroscopy, depending on the location of the fluorescent label within the probe.
  • the released nucleotides are separated from depolymerized probes, and the remaining probe or released nucleotide is fluorescently labeled.
  • Such an embodiment contemplates the provision of fluorescent labels and/or a magnetic nucleic acid separation medium. The above fluorescent embodiments contemplate that the fluorescent labels are distinguishable.
  • a kit has nucleic acid probes that comprise a non-natural nucleotide analog as an identifier nucleotide.
  • the depolymerization is assayed for using mass spectrometry .
  • the kit optionally further comprises instructions for detecting said nucleic acid by depolymerization.
  • the instructions present in such a kit instruct the user on how to use the components of the kit to perform the various methods of the present invention.
  • These instructions can include a description of the detection methods of the invention, including detection by luminescence spectroscopy, mass spectrometry, fluorescence spectroscopy, and absorbance spectroscopy.
  • the invention contemplates a kit for determining the presence or absence of a plurality of predetermined nucleic acid target sequences in a nucleic acid sample comprising the following components : an enzyme whose activity in the presence of pyrophosphate is to release identifier nucleotide as a nucleoside triphosphate from hybridized nucleic acid probe; pyrophosphate; and a plurality of nucleic acid probes, wherein the nucleic acid probes are complementary to their respective predetermined nucleic acid target sequence.
  • the enzyme whose activity in the presence of pyrophosphate is to release identifier nucleotide is as described hereinabove.
  • the plurality of nucleic acid probes are for related applications for a useful and convenient multiplex assay.
  • a useful and convenient multiplex assay For example, the detection of several genetic disease markers (e.g. Factor V Leiden and prothrombin) , a suite of human identity screens, the detection of a series of harmful microorganisms (e.g. certain E. coli strains , camphylobacter j ejuni , and salmonella or HIV- I, HIV-II, drug-resistant HIV-I, Hepatitis C and Hepatitis B) , or to check a plant for a series of nucleic acids.
  • genetic disease markers e.g. Factor V Leiden and prothrombin
  • a suite of human identity screens e.g. certain E. coli strains , camphylobacter j ejuni , and salmonella or HIV- I, HIV-II, drug-resistant HIV-I, Hepatitis C and Hepatitis B
  • the kit contains a plurality of nucleic acid probes for nucleic acid targets of interest.
  • each of the probes is designed to interrogate a different target DNA sequence .
  • the invention also contemplates kits containing instructions for use in interrogating the identity of a specific base within a nucleic acid target using a plurality of probes with different bases at the interrogation position and distinguishable probes.
  • the invention also contemplates kits containing instructions for use in simultaneously discriminating between two homologous nucleic acid targets that differ by one or more base pairs by providing a distinguishable probe for each target.
  • the invention contemplates a kit containing instructions for use in the simultaneous discrimination between a suite of nucleic acid targets that differ from a homologous nucleic acid target by one or more base pairs using distinguishable probes.
  • the invention further contemplates a kit containing instructions for use in determining whether a sample contains a plurality of nucleic acid targets having a deletion or insertion mutation.
  • the types of nucleic acid probes that can be included in the kits and their uses are described in greater detail below.
  • SNP single nucleotide polymorphism
  • Multiple probes designed to detect a mutant form of a gene in the CMV genome are used in one reaction and the signal from this reaction is compared to that from a probe that is specific for the non-mutated sequence.
  • the SNP sites are separated by only one base and the alleles are provided as pure nucleic acid target species.
  • CV20 (SEQ ID NO: 2) encode a segment of the CMV genome around position 1784 of the viral genome and these probes encode the non-mutant form of a gene.
  • Oligonucleotides CV21 (SEQ ID NO:3) and CV22 (SEQ ID NO:3) encode a segment of the CMV genome around position 1784 of the viral genome and these probes encode the non-mutant form of a gene.
  • Oligonucleotides CV23 (SEQ ID NO: 5) and CV24 (SEQ ID NO: 6) also encode the same genome segment as CV19 and CV20, but these oligonucleotides encode a form of the genome where the same Leu codon mutated in CV21 and CV22 is altered to a Phe codon. These oligonucleotides are used here as target nucleic acids for interrogation in this example. Oligonucleotide probe CV25 (SEQ ID NO: 7) exactly matches a region of CV19 and is designed to detect the non-mutated form of the gene.
  • Oligonucleotide probe CV26 (SEQ ID NO: 8) exactly matches a segment within CV21 and is designed to detect the version of the gene where the Leu codon has been mutated to a Ser codon.
  • Oligonucleotide probe CV27 (SEQ ID NO: 9) exactly matches a segment within CV24 and is designed to detect the version of the target where the Leu codon has been mutated to a Phe codon.
  • the target nucleic acid pairs CV19 and CV20, CV21 and CV22, and CV23 and CV24 were dissolved at 1 mg/mL in water, annealed by heating the solutions 95°C for 5 minutes and permitting to cool at room temperature for 10 minutes. Subsequently, the solutions were diluted to 3.3 ⁇ g/mL with water.
  • the probes CV25, CV26 and CV27 were dissolved at 1 mg/mL in water.
  • *Ratio is determined by dividing the signal from the wild type probe by the signal from the multiplexed mutant probes .
  • Multiple probes designed to detect a mutant form of two different target genes are used in one reaction, and the signal from this reaction is compared to that from a probe that is specific for one of the non-mutated sequences.
  • multiple SNP sites on multiple targets are interrogated in one reaction.
  • the targets and probes used in this study are: FV(l+2) (SEQ ID NO: 10 and SEQ ID NO: 11, respectively) FV(3+4) (SEQ ID NO: 12 and SEQ ID NO: 13, respectively), FV5 (SEQ ID NO:14), FV6 (SEQ ID NO:15), 9162 (SEQ ID N0.16), 9165 (SEQ ID NO:17), 9163 (SEQ ID NO:18), 9166 (SEQ ID NO:19), and CV2 (SEQ ID NO:20) .
  • a synthetic first nucleic acid target of the Factor V gene was designed to have the wild type sequence that contains a G at position 32 of FV1 (SEQ ID NO:10).
  • the complementary strand, FV2, (SEQ ID NO: 11) has 4 additional bases at its 3' terminus.
  • a second synthetic nucleic acid target of Factor V was designed to have the Leiden mutation, an A residue at position 32 of FV3.
  • the mutant complementary strand, FV4 also had 4 additional bases at its 3' terminus.
  • the nucleic acid target oligonucleotides, FV1 to FV4 were separately dissolved at a concentration of one mg/mL in water. Oligonucleotides 9162 and 9163 are complementary and have a segment of the wild type CMV genome.
  • Oligonucleotides 9163 and 9166 are complementary and have the same segment of the viral genome, but they contain a single base change present in a known drug resistant form of the virus. Equal volumes of one mg/mL 9162 and 9165 were combined to serve as wild type target for CMV. Equal volumes of one mg/mL 9163 and 9166 were combined to serve as the mutant target for CMV. Oligonucleotide CV2 represents an oligonucleotide designed to detect the drug resistant form of the CMV sequence .
  • All the target DNAs [FV(l+2), FV(3+4), 9162+9165, 9163+9166] were diluted to 0.3 ⁇ g/mL with water.
  • the other oligonucleotides were dissolved to 1 mg/mL with water.
  • the light values for the reactions were adjusted from the averaged plate values above by subtracting the average No-DNA signal value and target-alone averages and probe-alone values from the total light value measured for the various target and probe combinations. Reactions involving combinations of Target/Probe were further corrected by subtracting the appropriate adjusted probe-alone and target-alone values to yield a net light value. The resulting values are shown in the table below.
  • the system should give a very similar signal in the presence and absence of extraneous RNA.
  • the strength of the signal of probes designed to detect target globin mRNA in the presence of a large amount of yeast RNA is compared to the signal seen in the absence of added yeast RNA.
  • Hybridization solutions containing various levels of yeast RNA, Probe 6 (SEQ ID NO: 21) or Probe 8 (SEQ ID NO:22) and target globin mRNA (Gibco BRL, 18103-028) were assembled by adding 5 ⁇ L of a 500 ng/ ⁇ L solution of either probe 6 or probe 8 to 5 ⁇ L of a 40 ng/ ⁇ L solution of target globin mRNA and 10 ⁇ L yeast RNA (Sigma Chemical Co. R3629) in IX TE buffer (10 mM Tris, 1 mM EDTA) to produce solutions containing total amounts of yeast RNA of 0, 2, 20, 200, 400, and 800 ng. The solutions were heated at 50°C for 15 minutes and then permitted to cool to room temperature for 15.
  • the solution above was mixed and 18 ⁇ L of the mix were placed in 18 tubes. After cooling 15 minutes, 2 ⁇ L of the various hybridization solutions containing probe 6 were added to the tubes and the tubes were placed in a 37°C heating block.
  • thermostable enzymes to interrogate the CAH gene permits the interrogation of up to 6 multiple sites within one reaction.
  • the method used in this Example is illustrative of routine studies carried out in screening laboratories where usual results show the presence of an expected gene (or the absence of a mutant gene) in almost all of the samples, and only rarely shows the presence of a mutant gene. In the case illustrated here, a qualitative result is provided from which the exact mutation present can be determined in a subsequent assay.
  • Congenital adrenal hyperplasia is a group of autosomal recessive diseases resulting from a wide range of mutations in the steroid 21- hydroxylase (CYP21) gene that contains 10 exons . There is a high level of nucleic acid homology (98% in exons, 96% in introns) between CYP21, the functional gene, and CYP21P, the nonfunctional pseudogene.
  • the many types of mutations in this gene that can lead to disease include complete gene deletions, large gene conversions, single point mutations, and a small 8bp deletion [See, White, et al., Hum . Muta t . , 3:373-378, (1994)].
  • the majority of the CAH disease -causing mutations are sequences present in the nonexpressed CYP21P pseudogene, and arise in the CYP21 gene through recombination between CYP21P and CYP21. Thus, one mutation detection strategy specifically detects the CYP21 gene, and not the CYP21P pseudogene.
  • the frequency of disease-carrying alleles in the population is about 1 in 50.
  • Both wild type CAH PCR products, mutant synthetic targets, and a pseudogene PCR product amplified from the cloned CYP21P pseudogene were utilized as targets in this assay. They are listed below.
  • Primer pairs used in PCR amplification and the resulting products are as follows .
  • Synthetic targets and interrogation oligos utilized are listed below.
  • PCR reactions were assembled to amplify regions of the CAH gene with 4 different probe sets, using undigested human genomic DNA (Promega, G3041) as target (25 ng per reaction) .
  • human genomic DNA was predigested with the restriction enzyme Bel I, which specifically cleaves the CYP21 gene upstream of the forward PCR probe, thus permitting only amplification of CYP21P [Krone, Clinical Chem . 44 (10) : 2075-2082 (1998)].
  • the 2680 bp PCR product was amplified from 50 ng of digested DNA and subsequently cloned into the plasmid vector pGEM-T Easy (Promega, A1380) following the manufacturer's protocol. A clone was selected and sequenced (USB Sequenase kit, US70770) to confirm it was indeed the pseudogene.
  • the cloned CYP21P gene in the pGEM-T Easy vector was used in subsequent amplifications to obtain pure pseudogene PCR product for mutation interrogation analysis (100 pg of plasmid per PCR reaction) .
  • All 50 ⁇ L amplification reactions contained the following reagents: genomic DNA (as described above), IX reaction buffer (M1901) , 1.0 - 1.5 mM magnesium chloride (all with 1.0 mM except probe pair 10912+10911 for pseudogene, which contained 1.5 mM MgCl 2 ; Promega, A3511) , 200 ⁇ M each dNTP (C1141) , 50 pmoles each probe, and 2.5 units Taq DNA Polymerase (M1665) .
  • the exonuclease-treated DNA was eluted in 100 ⁇ L of nuclease-free water. Equal volumes of the CAH wild type (WT) 918 bp and 1496 bp PCR products were combined (to thus span the entire CAH gene) and interrogated either separately at each mutation site, or as a multiplexed group . Each interrogation assay (20 ⁇ L total volume) contained 4 ⁇ L of purified PCR product or 5 ng of synthetic target, and 1 ⁇ g interrogation oligo probe (or water for the no-oligo background control) . The reactions were incubated at 95°C for 3 minutes, followed by 10 minutes at 37°C for Klenow exo- or 55°C for Tne polymerase.
  • WT CAH wild type
  • the discrimination ratio was good both in the separate reactions for the combined PCR products, as well as the multiplexed reaction.
  • the multiplexed reaction using the CAH wild type PCR products and either 6 wild type interrogation oligo probes or 6 mutant interrogation oligo probes was combined with an equimolar amount of synthetic target (mutant synthetic target for each mutation site; 0.2 pmoles either PCR product or synthetic target) , to simulate a heterozygote sample.
  • thermostable enzymes Because of the large size of the CAH gene and the large number of different mutations that may be present, the use of the thermostable enzymes, and thus the increased stringency of the detection procedure, was found to be highly advantageous with this complex target. Mutation sites that interrogated poorly using Klenow exo- and yeast NDPK at 37°C, were more successfully interrogated when using the Tne triple mutant polymerase and Pfu NDPK at elevated temperatures. In addition, use of the thermostable enzymes permitted the multiplexing of numerous wild type or mutant interrogation oligos in the same interrogation assay, to obtain the rapid screening for mutations that may be present .
  • CAH forward primer 10910 5' CCTGTCCTTGGGAGACTAC 3' SEQ ID NO: 68 CAH forward primer (CYP21 only)
  • CAH interrogator oligo 6 wild type for mutation site 1
  • CAH interrogator oligo 7 wild type for mutation site 2
  • CAH interrogator oligo 8 wild type for mutation site 3
  • CAH interrogator oligo 4 (pseudogene/mutant) for mutation site 4
  • CAH interrogation oligo 24 (pseudogene/mutant) for mutation site 7
  • Target/probe hybrids were formed by combining 315 ng of the synthetic wild type CMV target oligonucleotide with either 10.5 ⁇ g wild type CMV probe for a matched hybrid, or 10.5 ⁇ g mutant CMV probe for a mismatched hybrid, and adding water to a final volume of 200 ⁇ L.
  • the oligonucleotides were CV 12 (SEQ ID NO:37), CV 15 (SEQ ID NO:38), and CV 16 (SEQ ID NO:39) .
  • CV12 (SEQ ID NO:37) is a single- stranded DNA segment of the genome of cytomegalovirus (CMV) in a form sensitive to the drug gancyclovir.
  • CV 15 (SEQ ID NO: 38) is a probe that hybridizes with total complementarity to the non-resistant CMV.
  • CV 16 (SEQ ID NO: 39) is identical to CV 15 (SEQ ID NO:38) except that it contains a one base change from the CV15 sequence at the site of the SNP that confers drug resistance to the virus. These solutions were heated to 95°C for at least 5 minutes, then cooled at room temperature for at least 10 minutes.
  • fractions containing the free dNTPs were collected and lyophilized. Fraction one contained dCTP, fraction two contained dGTP and TTP, and fraction three contained dATP.
  • each fraction was reconstituted in 100 ⁇ L of nanopure water.
  • Ten microliters of each fraction, or 10 ⁇ L of water as a control, were added to a 10 ⁇ L mixture of water, 10X DNA Polymerase Buffer, and ADP so that the final concentration was IX DNA pol buffer and 0.1 ⁇ M ADP.
  • NDPK (0.005 units) was added to each tube in one set of the tubes and an equal amount of water was added to each tube in the other set of tubes.
  • Samples and controls were incubated at 37°C for 15 minutes, 10 ⁇ L added to 100 ⁇ L of L/L reagent and the light output was measured on a Turner ® TDl ⁇ /20 luminometer.
  • the relative light units (rlu) results obtained are shown below:
  • fraction one match:mismatch ratio is 2.1
  • fraction 2 match : mismatch ratio is 2.2
  • fraction 3 match : mismatch ratio is 2.8.
  • the data therefore demonstrate the utility of using HPLC separation of individual nucleotides followed by NDPK conversion to ATP, the preferred substrate of luciferase.
  • Fraction 3 provides a slightly higher match:mismatch ratio owing to the presence of dATP in the nucleotide HPLC fraction. Nevertheless, HPLC separation of identifier nucleotides is useful in the interrogation assays of the present invention.
  • Example 6 Multiplex Determination of Nucleotide Sequences Associated with Factor V Leiden and with a Prothrombin SNP in the Same Reaction A assay is performed in this Example to determine if a human DNA sample contains the Leiden mutation of the Factor V gene, as well as a particular Prothrombin single nucleotide polymorphism
  • Probes PT5 (SEQ ID NO: 40) and PT6 (SEQ ID NO: 41) were used to PCR-amplify a region of human genomic DNA spanning about 500 base pairs encoding the prothrombin gene.
  • Probes 10861 (SEQ ID NO: 42) and 9828 (SEQ ID NO: 43) were used to PCR amplify a region of human genomic DNA spanning about 300 base pairs encoding the Factor V gene.
  • Probes PT5 and 10861 have phosphorothioate linkages between the first five bases at the 5' end.
  • the Factor V and Prothrombin fragments were co- amplified in one PCR reaction under the following conditions :
  • the PCR cycling parameters were as follows: 94°C, 2 minutes; (94°C, 30 seconds; 60°C, 1 minutes; 70°C, 1 minutes) x 40; 70°C, 5 minutes.
  • Fifty units of T7 gene 6 Exonuclease (USB Amersham) were added to 25 ⁇ L of the PCR reaction and the solution was incubated for 30 minutes at 37°C.
  • Magnetic silica (Promega, A1330) was used to remove free nucleotides from the solution and the remaining DNA was eluted with 100 ⁇ L of water.
  • the Prothrombin interrogation probes used are 11265 (SEQ ID NO: 44) that matches mutant prothrombin sequence and 11266 (SEQ ID NO: 45) that matches wild type prothrombin sequence. Each of those probes has a destabilizing mutation eight bases from the 3' end.
  • the Factor V interrogation probes used are 9919 (SEQ ID NO: 46) that matches wild types Factor V sequence and 11432 (SEQ ID NO: 47) that matches Factor V Leiden mutation sequence.
  • the reactions were incubated at 95°C for 3 minutes and then at 37°C for 10 minutes. Twenty microliters of the standard master mix was then added and the reaction incubated at 37°C for 15 minutes. One hundred microliters of the L/L reagent were then added and the light output measured in a Turner ® TD20/20 luminometer.
  • the master mix contains the following.
  • the light output was as follows
  • This equation is the analytical output from the interrogation including both wild type probes divided by the analytical output from both wild type probes added to the analytical output from both mutant probes. If that value is greater than 0.75 then the sample is homozygous wild type at both loci. If that value is less than 0.75 then there is good likelihood that at least one allele at least one of the loci is mutant and the sample should be further analyzed for the genotype at each locus separately.
  • This Example demonstrates that nucleotides released from the 3 ' -terminus of a hybridized probe in a multiplex reaction by a process of the invention can be detected by mass spectroscopy and thereby determine whether a mutant allele exists at one of the loci being studied.
  • Probes PT5 and 10861 have phosphorothioate linkages between the first five bases at the 5' end.
  • the PCR product is treated with T7 gene 6 Exonuclease (USB Amersham) and separated from free nucleotides as described in Example 6.
  • the Factor V interrogation probe, 11432 (SEQ ID NO:47), is totally complementary to a segment of the mutant Factor V Leiden mutation sequence. Each of these probes has a destabilizing mutation eight bases from the 3 ' -end.
  • the PCR products are synthesized, Exo 6 treated, and purified as described in Example 6.
  • the interrogation reactions are assembled with 40 ⁇ L of each PCR product and 1.5 nmol of each interrogation probe. Water is added to a final volume of 100 ⁇ L . These reactions are assembled in duplicate so that one can be assayed with Klenow exo- polymerase and yeast NDPK at 37°C, while the other is assayed with Tne triple mutant polymerase and Pfu NDPK at 70°C.
  • the two different master mixes are assembled. Both master mixes have 2 mM sodium pyrophosphate and 0.2 ⁇ M ADP. One with 1-2 U Klenow exo- and 0.2 U yeast NDPK, and 2X polymerase buffer (M195A) ; the other with 1 U Tne triple mutant polymerase and 0.1 U Pfu NDPK, 2X polymerase buffer (M1901) , and 5 mM magnesium chloride. An equal volume of each master mix is separately added to the reaction solutions described above.
  • An observance of released nucleotide from either of the reactions containing the two mutant probe, at levels greater than background, indicates the presence of a at least one mutant prothrombin or Factor V Leiden allele in the genomic DNA sample assayed.
  • Example 8 Multiplex Interrogation using
  • nucleotides released from the 3 ' -terminus of multiple probes, each hybridized to a target nucleic acid of interest, by a process of the invention can be detected by mass spectrometry or by fluorimetric HPLC and thereby provide evidence of the presence or absence of the target nucleic acid in a nucleic acid sample or of a specific base at an interrogation position of the target .
  • Each interrogation probe is designed to have a different fluorescent label attached to the 3 ' -terminal nucleotide in a manner such that the label does not interfere with the ability of the depolymerizing enzyme to remove the nucleotide from the probe.
  • fluorescent tags such as fluorescein or rhodamine, can be incorporated into the probe during synthesis with a fluorescent molecule attached to the phosphoramadite nucleotide with a linker of at least 6 carbons (Glen Research) .
  • Probes PT5 (SEQ ID NO: 40) and PT6 (SEQ ID NO:41) are used to PCR-amplify a region of human genomic DNA spanning about 500 base pairs encoding the prothrombin gene.
  • Probes 10861 (SEQ ID NO: 42) and 9828 (SEQ ID NO: 43) are used to PCR amplify a region of human genomic DNA spannning about 300 base pairs encoding the Factor V gene. These probes and the PCR reaction conditions are detailed in Example 6. The PCR products are treated with T7 gene 6 Exonuclease (USB Amersham) and separated from free nucleotides as described in Example 6.
  • the prothrombin interrogation probes are 11265 (SEQ ID NO:44), that is totally complementary to a segment of the mutant prothrombin sequence, and 11266 (SEQ ID NO:45), that is totally complementary to a segment of the wild-type prothrombin sequence.
  • Each of these probes has a destabilizing mutation eight bases from the 3 '-end.
  • each of these probes is synthesized with a fluorescent nucleotide analog at the 3 ' -terminal nucleotide position.
  • the prothrombin probes are tagged with fluorescein; the factor V probes are tagged with rhodamine.
  • the purified PCR products are interrogated in separate reactions with either both wild-type probes or both mutant probes. Interrogation reactions are assembled as follows: 40 ⁇ L each of the two PCR products
  • each of the wild type or each of the mutant labeled interrogation oligos water is added to a final volume of 100 ⁇ L.
  • the reactions are incubated at 95°C for 3 minutes and then at 37°C for 15 minutes.
  • the reactions are then lyophilized to a final volume of 20 ⁇ L. Twenty microliters of master mix are then added.
  • the composition of the master mix containing Klenow exo- is described in Example 4 with the exception that there is no ADP and no NDPK.
  • the reaction then proceeds at 37°C for 15 minutes.
  • the solutions are then split in half and analyzed using two different methods.
  • the presence or absence of released nucleotides in the solutions is analyzed by silicon desorption ionization mass spectroscopy (Wei, J. et al . Na ture . 399:243-246, 1999).
  • This method is sensitive to femtomole and attomole levels of analyte.
  • the samples are prepared for spectrometry as described in that paper. Essentially, analytes are dissolved in a deionized water/methanol mixture (1:1) at concentrations typically ranging from 0.001 to 10.0 ⁇ M. Aliquots (at least 0.5 to 1.0 ⁇ L, corresponding to at least 0.5 femtomol to 100 picomol analyte) of solution are deposited onto the porous surfaces and permitted to dry before mass spectrometry analysis.
  • DNA comprising a segment of the cytochrome B gene was amplified from a variety of animal species using PCR primers 11590 (SEQ ID NO:48) and 11589 (SEQ ID NO:49)
  • PCR primers were diluted in lOmM Tris, pH 7.5 , to a final concentration of 0.22 ⁇ g/ ⁇ L.
  • the genomic DNAs used were bovine (Clontech, 6850-1) , chicken (Clontech, 6852-1) , dog (Clontech, 6950-1) and human (Promega, G1521) .
  • the PCR reactions were assembled to include 5 ⁇ L 10X buffer with 15 mM MgCl 2 (Promega, M188J) , 1 ⁇ L dNTPs 10 mM (Promega, C144G) , 2 ⁇ L primer 11590, 2 ⁇ L primer 11589, 0.5 ⁇ L Taq polymerase 5U/ ⁇ L (Promega, M186E) , and 38.5 ⁇ L water. To each tube was then added 1 ⁇ L (100 ng) of genomic DNA. The PCR cycling parameters were (15 seconds, 94°C; 15 seconds, 55°C; 30 seconds, 72°C) x 30.
  • PCR products The size of PCR products was confirmed by running an aliquot on an agarose gel and visualizing with ethidium bromide (EtBr) staining. The PCR products were then separated from free nucleotides (Promega, A7170) and an aliquot run on an agarose gel. All samples produced a PCR product of the same size.
  • PCR DNA was then used in an assay to determine if it could be specifically identified with a species-specific probe.
  • One microliter of interrogation probe (l ⁇ g/ ⁇ L) and 17 ⁇ L water were combined with 2 ⁇ L of the appropriate PCR product and heated at 91°C for 3 minutes, then cooled at room temperature for 15 minutes.
  • Twenty microliters of master mix (described below) were added to each tube and each was further incubated at 37°C for 15 minutes.
  • Four microliters of the solutions were then added to 100 ⁇ L L/L reagent (Promega F120B) , and the relative light output (rlu) measured on a Turner ® TD20/20 luminometer. The rlu average values from two reactions, minus the DNA background values, along with the standard deviation values are listed below.
  • Both of the human-specific probes (11576 (SEQ ID NO:50) and 11583 (SEQ ID NO: 51) were shown to be specific for human mitochondrial DNA.
  • the cow-specific probe, 11588 (SEQ ID NO: 55) gave the best detection signal for cow DNA, but also detected the other species.
  • This Example illustrates use of a different type of oligonucleotide probe that is used to form a hairpin structure in the interrogation technology of this invention.
  • This study demonstrates a method for eliminating the need for adding a probe specific to the interrogation site to the interrogation reaction.
  • the oligonucleotide probe anneals to the target strand downstream of (3 ' to) the interrogation position in the target strand.
  • the oligonucleotide has at its 5' end an unannealed region of nucleotides followed by about 5 to about 20 nucleotides that are identical to the interrogation region on the target strand.
  • the annealed 3 ' end of the oligonucleotide is then extended through the interrogation position of the target strand creating what is referred to as extended probe.
  • the hybrid is denatured and a hairpin structure formed between the extended probe strand and the 5 ' end of the oligonucleotide probe. This region is then assayed in a standard interrogation reaction to determine if a mismatch is present or not.
  • probes were designed to represent different types of hairpin formations that an extended probe strands may assume. These probes are 10207 (SEQ ID NO:57) , 10208 (SEQ ID NO:58) , 10209 (SEQ ID NO:59), and 10212 (SEQ ID NO:60). These probes are predicted to form the following self-hybridized secondary structures when allowed to self-anneal:
  • a 5 ⁇ L (5 ⁇ g) aliquot of each of the four probes was diluted to 100 ⁇ L with nanopure water. They were then sequentially diluted 1:10 to a final dilution factor of 1:100,000. Twenty microliters of the diluted probes were heated, in separate tubes, at 95°C for 3 minutes and cooled to room temperature for 10 minutes to permit self- annealing. The following master mix was assembled and mixed.
  • Probe 10207 worked as an efficient target for interrogation as expected, with probe 10208 providing the anticipated negative results.
  • Probe 10212 has only a three base match so it may be un- extended, thus resulting in the low values.
  • Probe 10209 likely has the 3' terminal nucleotide unannealed when the hairpin forms due to the mismatch at the third nucleotide in from the 3' end. Such an unannealed 3 ' terminal nucleotide would account for the low rlu values.
  • Fig. 2 illustrate use of a different type of oligonucleotide probe, a "REAPERTM” probe in a process of this invention.
  • This example demonstrates a method for eliminating the need for adding a probe specific to the interrogation site to the interrogation reaction.
  • the oligonucleotide first probe SEQ ID NO: 62
  • anneals to the target strand SEQ ID NO: 61
  • Fig. 2A the interrogation position in the target strand
  • the probe has at its 5 ' -end an unannealed region of nucleotides including about 5 to about 20 nucleotides that are identical to a region on the target strand including the interrogation position. This region of identity is present in the same orientation on both the target and the probe strands.
  • the annealed 3 ' -end of the probe is then extended through the interrogation position of the target strand forming what is referred to as a first extended probe and an extended first hybrid as is illustrated in Fig.2B (SEQ ID NO:63).
  • the extended first hybrid is denatured and a second probe (SEQ ID NO: 64) is annealed to the first extended probe to form a second hybrid. This second probe is complementary to the first extended probe strand at a region downstream of the interrogation position on the first extended probe strand (Fig. 2C) .
  • the second probe is then extended and a second extended hybrid is formed as illustrated in Fig. 2D.
  • the second extended hybrid is comprised of the first extended probe and second extended probe
  • the strands of the second extended hybrid are denatured and permitted to renature to form a hairpin structure.
  • the first extended probe forms a hairpin structure that has a
  • the second extended probe forms a hairpin structure that contains a 5 ' -overhang that provides a substrate for depolymerization.
  • the second extended probe strand is then depolymerized and the analytical output obtained as described elsewhere herein.
  • the analytical output determines the presence or absence of the original target strand or of a particular base in the original target strand as is also discussed elsewhere herein.
  • SEQ ID NO: 61 oligonucleotide is diluted to 1 mg/mL in water. This solution is labeled 286.
  • SEQ ID NO: 62 oligonucleotide is diluted to 1 mg/mL in water and this solution is labeled 287.
  • One microliter of each solution 286 and 287 is combined with 18 ⁇ L water. The solution is heated to 95°C for 5 minutes then is cooled at room temperature for 10 minutes to permit oligonucleotides of SEQ ID NOs:61 and 62 to anneal.
  • dNTP mixture to a final concentration of 0.25 mM for each dNTP, 10X Klenow buffer to a final concentration of IX, and 5 U of Klenow enzyme.
  • the tube with these components is incubated at 37°C for 30 minutes.
  • the extended first hybrid DNA so formed (containing SEQ ID NO: 63) is purified (Qiagen, Mermaid system) and eluted into 50 ⁇ l of water.
  • the SEQ ID NO: 65/63 second extended hybrid DNA (Fig. 2D) formed is purified (Qiagen, Mermaid system) to separate the extended hybrid from the unreacted dNTPs and eluted into 50 ⁇ l water.
  • the original 287 oligo is biotinylated at it's 5 ' -end and this biotin is then also present in strand of SEQ ID NO: 63.
  • This biotinylated strand 288 is then denatured from strand 290 and removed from the solution with streptavidin coated paramagnetic particles according to the manufacturer's instructions (Promega, Z5481) and the 290 hairpin structure is allowed to form as below) .
  • This hybrid solution is then heated to 95°C for 5 minutes diluted to 100 ⁇ l with water and is cooled on ice for 10 minutes to permit hairpin structure formation.
  • a master mix is assembled and mixed according to the following table .

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Abstract

L'invention concerne des procédés utilisant la dépolymérisation d'un hybride d'acide nucléique pour analyser qualitativement et quantitativement la présence de séquences cibles d'acides nucléiques prédéterminées au moyen d'une méthode de dosage multiplex. Les applications de ces procédés comprennent la détection de polymorphismes de nucléotides simples, l'identification de changements de bases simples, la spéciation, le génotypage, les diagnostics de marqueurs médicaux, et les applications associées.
PCT/US2000/004243 1999-02-18 2000-02-18 Procede multiplex de detection d'acides nucleiques WO2000049181A1 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
AU30019/00A AU774085B2 (en) 1999-02-18 2000-02-18 Multiplex method for nucleic acid detection
EP00908726A EP1155150A1 (fr) 1999-02-18 2000-02-18 Procede multiplex de detection d'acides nucleiques
CA002357011A CA2357011A1 (fr) 1999-02-18 2000-02-18 Procede multiplex de detection d'acides nucleiques
JP2000599904A JP2003535568A (ja) 1999-02-18 2000-02-18 核酸検出のための多重法

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US09/252,436 US6159693A (en) 1998-03-13 1999-02-18 Nucleic acid detection
USPCT/US99/05304 1999-03-11
PCT/US1999/005304 WO1999046409A1 (fr) 1998-03-13 1999-03-11 Detection d'acide nucleique
US09/358,972 US6235480B1 (en) 1998-03-13 1999-07-21 Detection of nucleic acid hybrids
US09/406,064 1999-09-27
US09/252,436 1999-09-27
US09/358,972 1999-09-27
US09/406,064 US6270973B1 (en) 1998-03-13 1999-09-27 Multiplex method for nucleic acid detection

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WO2002063049A2 (fr) * 2001-02-02 2002-08-15 Genome Therapeutics Corporation Methodes de determination d'un nucleotide a un emplacement specifique dans une molecule d'acide nucleique
WO2003102179A1 (fr) * 2002-05-31 2003-12-11 Kankyo Engineering Co., Ltd. Nouveau procede de dosage d'acide nucleique au moyen d'un nucleotide marque
JP2004524856A (ja) * 2001-05-09 2004-08-19 イギリス国 分析方法およびキット
US7090975B2 (en) 1998-03-13 2006-08-15 Promega Corporation Pyrophosphorolysis and incorporation of nucleotide method for nucleic acid detection
WO2014093291A1 (fr) * 2012-12-10 2014-06-19 Advandx, Inc. Utilisation de sondes pour l'identification par spectrométrie de masse de micro-organismes ou de cellules et de pathologies associées présentant un intérêt

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WO2003102179A1 (fr) * 2002-05-31 2003-12-11 Kankyo Engineering Co., Ltd. Nouveau procede de dosage d'acide nucleique au moyen d'un nucleotide marque
WO2014093291A1 (fr) * 2012-12-10 2014-06-19 Advandx, Inc. Utilisation de sondes pour l'identification par spectrométrie de masse de micro-organismes ou de cellules et de pathologies associées présentant un intérêt

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EP1155150A1 (fr) 2001-11-21

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